Canonical Allele Identifier: CA1675959416

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114849_158114851delinsATT , CM000668.2:g.158114849_158114851delinsATT	GRCh38
NC_000006.11:g.158535881_158535883delinsATT , CM000668.1:g.158535881_158535883delinsATT	GRCh37
NC_000006.10:g.158455869_158455871delinsATT	NCBI36
NG_032889.1:g.58430_58432delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.834_836delinsAAT	ENSP00000391168.2:n.834_836delinsAAT
ENST00000607071.6:c.*1342_*1344delinsAAT	ENSP00000475855.1:n.*1342_*1344delinsAAT
ENST00000642244.1:c.1532_1534delinsAAT	ENSP00000493554.1:p.Glu511=
ENST00000642903.1:c.1622_1624delinsAAT	ENSP00000493559.1:p.Glu541=
ENST00000644972.1:c.1622_1624delinsAAT	ENSP00000496451.1:p.Glu541=
ENST00000645077.1:c.*1243_*1245delinsAAT	ENSP00000496113.1:n.*1243_*1245delinsAAT
ENST00000645172.1:c.*1324_*1326delinsAAT	ENSP00000495367.1:n.*1324_*1326delinsAAT
ENST00000646190.1:n.2953_2955delinsAAT
ENST00000646208.1:c.1358_1360delinsAAT	ENSP00000493723.1:p.Glu453=
ENST00000646410.1:c.1493_1495delinsAAT	ENSP00000494205.1:p.Glu498=
ENST00000646562.1:c.*1456_*1458delinsAAT	ENSP00000496087.1:n.*1456_*1458delinsAAT
ENST00000647468.2:c.1622_1624delinsAAT MANE Select	ENSP00000496731.1:p.Glu541=
ENST00000648111.1:c.*1310_*1312delinsAAT	ENSP00000497275.1:n.*1310_*1312delinsAAT
ENST00000367101.5:c.*70_*72delinsAAT	ENSP00000356068.1:n.*70_*72delinsAAT
ENST00000367104.7:c.1622_1624delinsAAT	ENSP00000356071.3:p.Glu541=
ENST00000435180.5:c.347_349delinsAAT	ENSP00000391168.1:p.Glu116=
ENST00000606965.5:c.*183_*185delinsAAT	ENSP00000475808.1:n.*183_*185delinsAAT
ENST00000607071.5:c.*1556_*1558delinsAAT	ENSP00000475855.1:n.*1556_*1558delinsAAT
ENST00000607742.5:c.*2900_*2902delinsAAT	ENSP00000475523.1:n.*2900_*2902delinsAAT
NM_032861.3:c.1622_1624delinsAAT	NP_116250.3:p.Glu541=
NR_073096.1:n.1555_1557delinsAAT
XM_006715586.1:c.1412_1414delinsAAT	XP_006715649.1:p.Glu471=
XM_011536196.1:c.1601_1603delinsAAT	XP_011534498.1:p.Glu534=
XM_011536197.1:c.1508_1510delinsAAT	XP_011534499.1:p.Glu503=
XM_011536198.1:c.1412_1414delinsAAT	XP_011534500.1:p.Glu471=
XM_006715586.3:c.1412_1414delinsAAT	XP_006715649.1:p.Glu471=
XM_011536196.3:c.1601_1603delinsAAT	XP_011534498.1:p.Glu534=
XM_011536198.3:c.1412_1414delinsAAT	XP_011534500.1:p.Glu471=
XM_024446573.1:c.1622_1624delinsAAT	XP_024302341.1:p.Glu541=
XR_001743697.2:n.1653_1655delinsAAT
XR_942606.2:n.1704_1706delinsAAT
NM_032861.4:c.1622_1624delinsAAT MANE Select	NP_116250.3:p.Glu541=
NR_073096.2:n.1537_1539delinsAAT