Canonical Allele Identifier: CA2695207272

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114869_158114885dup , CM000668.2:g.158114869_158114885dup	GRCh38
NC_000006.11:g.158535901_158535917dup , CM000668.1:g.158535901_158535917dup	GRCh37
NC_000006.10:g.158455889_158455905dup	NCBI36
NG_032889.1:g.58397_58413dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.801_817dup	ENSP00000391168.2:n.801_817dup
ENST00000607071.6:c.*1309_*1325dup	ENSP00000475855.1:n.*1309_*1325dup
ENST00000642244.1:c.1499_1515dup	ENSP00000493554.1:p.Gly506IlefsTer?
ENST00000642903.1:c.1589_1605dup	ENSP00000493559.1:p.Gly536IlefsTer?
ENST00000644972.1:c.1589_1605dup	ENSP00000496451.1:p.Gly536IlefsTer?
ENST00000645077.1:c.*1210_*1226dup	ENSP00000496113.1:n.*1210_*1226dup
ENST00000645172.1:c.*1291_*1307dup	ENSP00000495367.1:n.*1291_*1307dup
ENST00000646190.1:n.2920_2936dup
ENST00000646208.1:c.1325_1341dup	ENSP00000493723.1:p.Gly448IlefsTer?
ENST00000646410.1:c.1460_1476dup	ENSP00000494205.1:p.Gly493IlefsTer?
ENST00000646562.1:c.*1423_*1439dup	ENSP00000496087.1:n.*1423_*1439dup
ENST00000647468.2:c.1589_1605dup MANE Select	ENSP00000496731.1:p.Gly536IlefsTer?
ENST00000648111.1:c.*1277_*1293dup	ENSP00000497275.1:n.*1277_*1293dup
ENST00000367101.5:c.*37_*53dup	ENSP00000356068.1:n.*37_*53dup
ENST00000367104.7:c.1589_1605dup	ENSP00000356071.3:p.Gly536IlefsTer?
ENST00000435180.5:c.314_330dup	ENSP00000391168.1:p.Gly111IlefsTer?
ENST00000606965.5:c.*150_*166dup	ENSP00000475808.1:n.*150_*166dup
ENST00000607071.5:c.*1523_*1539dup	ENSP00000475855.1:n.*1523_*1539dup
ENST00000607742.5:c.*2867_*2883dup	ENSP00000475523.1:n.*2867_*2883dup
NM_032861.3:c.1589_1605dup	NP_116250.3:p.Gly536IlefsTer?
NR_073096.1:n.1522_1538dup
XM_006715586.1:c.1379_1395dup	XP_006715649.1:p.Gly466IlefsTer?
XM_011536196.1:c.1568_1584dup	XP_011534498.1:p.Gly529IlefsTer?
XM_011536197.1:c.1475_1491dup	XP_011534499.1:p.Gly498IlefsTer?
XM_011536198.1:c.1379_1395dup	XP_011534500.1:p.Gly466IlefsTer?
XM_006715586.3:c.1379_1395dup	XP_006715649.1:p.Gly466IlefsTer?
XM_011536196.3:c.1568_1584dup	XP_011534498.1:p.Gly529IlefsTer?
XM_011536198.3:c.1379_1395dup	XP_011534500.1:p.Gly466IlefsTer?
XM_024446573.1:c.1589_1605dup	XP_024302341.1:p.Gly536IlefsTer?
XR_001743697.2:n.1620_1636dup
XR_942606.2:n.1671_1687dup
NM_032861.4:c.1589_1605dup MANE Select	NP_116250.3:p.Gly536IlefsTer?
NR_073096.2:n.1504_1520dup