Canonical Allele Identifier: CA1675959474

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114922C= , CM000668.2:g.158114922C=	GRCh38
NC_000006.11:g.158535954C= , CM000668.1:g.158535954C=	GRCh37
NC_000006.10:g.158455942C=	NCBI36
NG_032889.1:g.58359G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.763G=	ENSP00000391168.2:n.763G=
ENST00000607071.6:c.*1271G=	ENSP00000475855.1:n.*1271G=
ENST00000642244.1:c.1461G=	ENSP00000493554.1:p.Met487=
ENST00000642903.1:c.1551G=	ENSP00000493559.1:p.Met517=
ENST00000644972.1:c.1551G=	ENSP00000496451.1:p.Met517=
ENST00000645077.1:c.*1172G=	ENSP00000496113.1:n.*1172G=
ENST00000645172.1:c.*1253G=	ENSP00000495367.1:n.*1253G=
ENST00000646190.1:n.2882G=
ENST00000646208.1:c.1287G=	ENSP00000493723.1:p.Met429=
ENST00000646410.1:c.1422G=	ENSP00000494205.1:p.Met474=
ENST00000646562.1:c.*1385G=	ENSP00000496087.1:n.*1385G=
ENST00000647468.2:c.1551G= MANE Select	ENSP00000496731.1:p.Met517=
ENST00000648111.1:c.*1239G=	ENSP00000497275.1:n.*1239G=
ENST00000367101.5:c.1595G=	ENSP00000356068.1:p.Ter532=
ENST00000367104.7:c.1551G=	ENSP00000356071.3:p.Met517=
ENST00000435180.5:c.276G=	ENSP00000391168.1:p.Met92=
ENST00000606965.5:c.*112G=	ENSP00000475808.1:n.*112G=
ENST00000607071.5:c.*1485G=	ENSP00000475855.1:n.*1485G=
ENST00000607742.5:c.*2829G=	ENSP00000475523.1:n.*2829G=
NM_032861.3:c.1551G=	NP_116250.3:p.Met517=
NR_073096.1:n.1484G=
XM_006715586.1:c.1341G=	XP_006715649.1:p.Met447=
XM_011536196.1:c.1530G=	XP_011534498.1:p.Met510=
XM_011536197.1:c.1437G=	XP_011534499.1:p.Met479=
XM_011536198.1:c.1341G=	XP_011534500.1:p.Met447=
XM_006715586.3:c.1341G=	XP_006715649.1:p.Met447=
XM_011536196.3:c.1530G=	XP_011534498.1:p.Met510=
XM_011536198.3:c.1341G=	XP_011534500.1:p.Met447=
XM_024446573.1:c.1551G=	XP_024302341.1:p.Met517=
XR_001743697.2:n.1582G=
XR_942606.2:n.1633G=
NM_032861.4:c.1551G= MANE Select	NP_116250.3:p.Met517=
NR_073096.2:n.1466G=