Canonical Allele Identifier: CA1675955800

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146874G= , CM000668.2:g.158146874G=	GRCh38
NC_000006.11:g.158567906G= , CM000668.1:g.158567906G=	GRCh37
NC_000006.10:g.158487894G=	NCBI36
NG_032889.1:g.26407C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*229C=	ENSP00000475855.1:n.*229C=
ENST00000642244.1:c.305C=	ENSP00000493554.1:p.Ala102=
ENST00000642903.1:c.395C=	ENSP00000493559.1:p.Ala132=
ENST00000643093.1:n.445C=
ENST00000644972.1:c.395C=	ENSP00000496451.1:p.Ala132=
ENST00000645077.1:c.*229C=	ENSP00000496113.1:n.*229C=
ENST00000645172.1:c.*189+1991C=	ENSP00000495367.1:n.*189+1991C=
ENST00000646190.1:n.1626C=
ENST00000646208.1:c.131C=	ENSP00000493723.1:p.Ala44=
ENST00000646410.1:c.266C=	ENSP00000494205.1:p.Ala89=
ENST00000646562.1:c.*229C=	ENSP00000496087.1:n.*229C=
ENST00000647468.2:c.395C= MANE Select	ENSP00000496731.1:p.Ala132=
ENST00000648111.1:c.*39C=	ENSP00000497275.1:n.*39C=
ENST00000367101.5:c.395C=	ENSP00000356068.1:p.Ala132=
ENST00000367104.7:c.395C=	ENSP00000356071.3:p.Ala132=
ENST00000606965.5:c.395C=	ENSP00000475808.1:p.Ala132=
ENST00000607000.1:c.395C=	ENSP00000475788.1:p.Ala132=
ENST00000607071.5:c.*229C=	ENSP00000475855.1:n.*229C=
ENST00000607742.5:c.*229C=	ENSP00000475523.1:n.*229C=
NM_032861.3:c.395C=	NP_116250.3:p.Ala132=
NR_073096.1:n.537C=
XM_006715586.1:c.185C=	XP_006715649.1:p.Ala62=
XM_011536196.1:c.374C=	XP_011534498.1:p.Ala125=
XM_011536197.1:c.395C=	XP_011534499.1:p.Ala132=
XM_011536198.1:c.185C=	XP_011534500.1:p.Ala62=
XR_942606.1:n.396C=
XM_006715586.3:c.185C=	XP_006715649.1:p.Ala62=
XM_011536196.3:c.374C=	XP_011534498.1:p.Ala125=
XM_011536198.3:c.185C=	XP_011534500.1:p.Ala62=
XM_024446573.1:c.395C=	XP_024302341.1:p.Ala132=
XR_001743697.2:n.476C=
XR_942606.2:n.527C=
NM_032861.4:c.395C= MANE Select	NP_116250.3:p.Ala132=
NR_073096.2:n.519C=