Canonical Allele Identifier: CA368231188

Gene: SGCE CASD1

Linked Data

• MyVariant Identifiers: chr7:g.94230117C>A (hg19) ; chr7:g.94600805C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.94600805C>A , CM000669.2:g.94600805C>A	GRCh38
NC_000007.13:g.94230117C>A , CM000669.1:g.94230117C>A	GRCh37
NC_000007.12:g.94068053C>A	NCBI36
NG_008893.1:g.60405G>T
NG_008893.2:g.60405G>T
NG_008893.3:g.60768G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415788.3:c.986G>T (SGCE)	ENSP00000405313.2:p.Gly329Val
ENST00000428696.7:c.857G>T (SGCE)	ENSP00000397536.3:p.Gly286Val
ENST00000437425.7:c.755G>T (SGCE)	ENSP00000394061.2:p.Gly252Val
ENST00000445866.7:c.878G>T (SGCE)	ENSP00000398930.2:p.Gly293Val
ENST00000447873.6:c.878G>T (SGCE)	ENSP00000388734.1:p.Gly293Val
ENST00000642169.1:c.*260G>T (SGCE)	ENSP00000496346.1:n.*260G>T
ENST00000642291.1:c.739G>T (SGCE)
ENST00000642353.1:n.849G>T (SGCE)
ENST00000642394.1:c.755G>T (SGCE)	ENSP00000493751.1:p.Gly252Val
ENST00000642441.1:c.959G>T (SGCE)	ENSP00000495994.1:p.Gly320Val
ENST00000642497.1:n.1651G>T (SGCE)
ENST00000642564.1:n.978G>T (SGCE)
ENST00000642638.1:c.*916G>T (SGCE)	ENSP00000495555.1:n.*916G>T
ENST00000642707.1:c.986G>T (SGCE)	ENSP00000495270.1:p.Gly329Val
ENST00000642754.1:n.5750G>T (SGCE)
ENST00000642759.1:n.967G>T (SGCE)
ENST00000642802.1:n.700G>T (SGCE)
ENST00000642904.1:n.966G>T (SGCE)
ENST00000642933.1:c.878G>T (SGCE)	ENSP00000496237.1:p.Gly293Val
ENST00000643020.1:c.804G>T (SGCE)
ENST00000643041.1:c.878G>T (SGCE)	ENSP00000495311.1:p.Gly293Val
ENST00000643128.1:c.878G>T (SGCE)	ENSP00000496678.1:p.Gly293Val
ENST00000643160.1:c.109G>T (SGCE)
ENST00000643193.1:c.878G>T (SGCE)	ENSP00000496559.1:p.Gly293Val
ENST00000643206.1:c.*459G>T (SGCE)	ENSP00000496172.1:n.*459G>T
ENST00000643272.1:c.986G>T (SGCE)	ENSP00000494488.1:p.Gly329Val
ENST00000643324.1:n.1769G>T (SGCE)
ENST00000643491.1:n.806G>T (SGCE)
ENST00000643568.1:c.559G>T (SGCE)
ENST00000643605.1:c.*865G>T (SGCE)	ENSP00000496480.1:n.*865G>T
ENST00000643610.1:c.878G>T (SGCE)	ENSP00000494350.1:p.Gly293Val
ENST00000643714.1:n.946G>T (SGCE)
ENST00000643903.1:c.878G>T (SGCE)	ENSP00000495165.1:p.Gly293Val
ENST00000643991.1:c.787G>T (SGCE)
ENST00000644087.1:c.*955G>T (SGCE)	ENSP00000495249.1:n.*955G>T
ENST00000644116.1:c.878G>T (SGCE)	ENSP00000495276.1:p.Gly293Val
ENST00000644122.1:c.959G>T (SGCE)	ENSP00000495236.1:p.Gly320Val
ENST00000644201.1:c.661G>T (SGCE)	ENSP00000495044.1:n.661G>T
ENST00000644268.1:n.1498G>T (SGCE)
ENST00000644373.1:n.1914G>T (SGCE)
ENST00000644375.1:c.944G>T (SGCE)	ENSP00000494315.1:p.Gly315Val
ENST00000644533.1:n.1633G>T (SGCE)
ENST00000644551.1:c.959G>T (SGCE)	ENSP00000493981.1:p.Gly320Val
ENST00000644609.1:c.878G>T (SGCE)	ENSP00000496045.1:p.Gly293Val
ENST00000644639.1:c.*539G>T (SGCE)	ENSP00000496391.1:n.*539G>T
ENST00000644658.1:c.390-1082G>T (SGCE)
ENST00000644674.1:n.779G>T (SGCE)
ENST00000644681.1:c.605G>T (SGCE)	ENSP00000496455.1:p.Gly202Val
ENST00000644682.1:c.942G>T (SGCE)
ENST00000644816.1:c.878G>T (SGCE)	ENSP00000494898.1:p.Gly293Val
ENST00000644966.1:c.857G>T (SGCE)	ENSP00000495105.1:n.857G>T
ENST00000645101.1:c.1067G>T (SGCE)	ENSP00000494975.1:p.Gly356Val
ENST00000645109.1:c.986G>T (SGCE)	ENSP00000495931.1:p.Gly329Val
ENST00000645262.1:c.755G>T (SGCE)	ENSP00000494164.1:p.Gly252Val
ENST00000645445.1:c.852G>T (SGCE)
ENST00000645535.1:c.605G>T (SGCE)	ENSP00000493984.1:p.Gly202Val
ENST00000645579.1:n.1798G>T (SGCE)
ENST00000645624.1:n.441G>T (SGCE)
ENST00000645725.1:c.959G>T (SGCE)	ENSP00000495480.1:p.Gly320Val
ENST00000646098.1:c.854G>T (SGCE)	ENSP00000495591.1:p.Gly285Val
ENST00000646119.1:c.852G>T (SGCE)
ENST00000646137.1:c.878G>T (SGCE)	ENSP00000495199.1:p.Gly293Val
ENST00000646265.1:c.967G>T (SGCE)
ENST00000646301.1:c.851G>T (SGCE)
ENST00000646434.1:c.1127G>T (SGCE)
ENST00000646466.1:c.*808G>T (SGCE)	ENSP00000493511.1:n.*808G>T
ENST00000646489.1:c.986G>T (SGCE)	ENSP00000496268.1:p.Gly329Val
ENST00000646559.1:c.*808G>T (SGCE)	ENSP00000495838.1:n.*808G>T
ENST00000646600.1:c.*808G>T (SGCE)	ENSP00000494041.1:n.*808G>T
ENST00000646682.1:c.*486G>T (SGCE)	ENSP00000496461.1:n.*486G>T
ENST00000646879.1:c.878G>T (SGCE)	ENSP00000495209.1:p.Gly293Val
ENST00000646910.1:n.911G>T (SGCE)
ENST00000646943.1:c.878G>T (SGCE)	ENSP00000494666.1:p.Gly293Val
ENST00000647018.1:c.986G>T (SGCE)	ENSP00000493722.1:p.Gly329Val
ENST00000647031.1:n.3492G>T (SGCE)
ENST00000647048.1:c.702G>T (SGCE)
ENST00000647096.1:c.986G>T (SGCE)	ENSP00000494192.1:p.Gly329Val
ENST00000647110.1:c.884G>T (SGCE)	ENSP00000494738.1:p.Gly295Val
ENST00000647334.1:c.984G>T (SGCE)
ENST00000647351.1:c.959G>T (SGCE)	ENSP00000494556.1:p.Gly320Val
ENST00000647379.1:n.91G>T (SGCE)
ENST00000647533.1:n.1577G>T (SGCE)
ENST00000648936.2:c.878G>T (SGCE) MANE Select	ENSP00000497130.1:p.Gly293Val
ENST00000265735.11:c.878G>T (SGCE)	ENSP00000265735.6:p.Gly293Val
ENST00000415788.2:c.986G>T (SGCE)	ENSP00000405313.2:p.Gly329Val
ENST00000428696.6:c.878G>T (SGCE)	ENSP00000397536.2:p.Gly293Val
ENST00000437425.6:c.755G>T (SGCE)	ENSP00000394061.2:p.Gly252Val
ENST00000445866.6:c.878G>T (SGCE)	ENSP00000398930.2:p.Gly293Val
ENST00000447873.5:c.878G>T (SGCE)	ENSP00000388734.1:p.Gly293Val
ENST00000462731.1:n.171G>T (SGCE)
NM_001099400.1:c.878G>T (SGCE)	NP_001092870.1:p.Gly293Val
NM_001099401.1:c.878G>T (SGCE)	NP_001092871.1:p.Gly293Val
NM_001301139.1:c.755G>T (SGCE)	NP_001288068.1:p.Gly252Val
NM_003919.2:c.878G>T (SGCE)	NP_003910.1:p.Gly293Val
XM_005250675.3:c.986G>T (SGCE)	XP_005250732.1:p.Gly329Val
XM_005250677.3:c.986G>T (SGCE)	XP_005250734.1:p.Gly329Val
XM_011516495.1:c.2128-30511C>A (CASD1)	XP_011514797.1:n.2128-30511C>A
XM_011516663.1:c.986G>T (SGCE)	XP_011514965.1:p.Gly329Val
XM_011516664.1:c.986G>T (SGCE)	XP_011514966.1:p.Gly329Val
XM_011516665.1:c.878G>T (SGCE)	XP_011514967.1:p.Gly293Val
XM_011516666.1:c.878G>T (SGCE)	XP_011514968.1:p.Gly293Val
XM_011516667.1:c.791G>T (SGCE)	XP_011514969.1:p.Gly264Val
XM_011516668.1:c.755G>T (SGCE)	XP_011514970.1:p.Gly252Val
XM_011516669.1:c.605G>T (SGCE)	XP_011514971.1:p.Gly202Val
NM_001346713.1:c.986G>T (SGCE)	NP_001333642.1:p.Gly329Val
NM_001346715.1:c.986G>T (SGCE)	NP_001333644.1:p.Gly329Val
NM_001346717.1:c.878G>T (SGCE)	NP_001333646.1:p.Gly293Val
NM_001346719.1:c.791G>T (SGCE)	NP_001333648.1:p.Gly264Val
NM_001346720.1:c.605G>T (SGCE)	NP_001333649.1:p.Gly202Val
NM_001362807.1:c.791G>T (SGCE)	NP_001349736.1:p.Gly264Val
NM_001362808.1:c.605G>T (SGCE)	NP_001349737.1:p.Gly202Val
NM_001362809.1:c.755G>T (SGCE)	NP_001349738.1:p.Gly252Val
XM_011516495.2:c.2128-30511C>A (CASD1)	XP_011514797.1:n.2128-30511C>A
XM_011516663.2:c.986G>T (SGCE)	XP_011514965.1:p.Gly329Val
XM_011516664.2:c.986G>T (SGCE)	XP_011514966.1:p.Gly329Val
XM_011516665.3:c.878G>T (SGCE)	XP_011514967.1:p.Gly293Val
XM_011516666.3:c.878G>T (SGCE)	XP_011514968.1:p.Gly293Val
XM_011516667.2:c.791G>T (SGCE)	XP_011514969.1:p.Gly264Val
XM_011516669.3:c.605G>T (SGCE)	XP_011514971.1:p.Gly202Val
XM_017012763.1:c.791G>T (SGCE)	XP_016868252.1:p.Gly264Val
XM_017012767.1:c.605G>T (SGCE)	XP_016868256.1:p.Gly202Val
XM_024446985.1:c.755G>T (SGCE)	XP_024302753.1:p.Gly252Val
XM_024446986.1:c.755G>T (SGCE)	XP_024302754.1:p.Gly252Val
NM_001099400.2:c.878G>T (SGCE)	NP_001092870.1:p.Gly293Val
NM_001099401.2:c.878G>T (SGCE)	NP_001092871.1:p.Gly293Val
NM_001301139.2:c.755G>T (SGCE)	NP_001288068.1:p.Gly252Val
NM_001346713.2:c.986G>T (SGCE)	NP_001333642.1:p.Gly329Val
NM_001346715.2:c.986G>T (SGCE)	NP_001333644.1:p.Gly329Val
NM_001346717.2:c.878G>T (SGCE)	NP_001333646.1:p.Gly293Val
NM_001346719.2:c.791G>T (SGCE)	NP_001333648.1:p.Gly264Val
NM_001346720.2:c.605G>T (SGCE)	NP_001333649.1:p.Gly202Val
NM_001362807.2:c.791G>T (SGCE)	NP_001349736.1:p.Gly264Val
NM_001362808.2:c.605G>T (SGCE)	NP_001349737.1:p.Gly202Val
NM_001362809.2:c.755G>T (SGCE)	NP_001349738.1:p.Gly252Val
NM_003919.3:c.878G>T (SGCE) MANE Select	NP_003910.1:p.Gly293Val