Canonical Allele Identifier: CA1242197372

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529323C= , CM000664.2:g.31529323C=	GRCh38
NC_000002.11:g.31754393C= , CM000664.1:g.31754393C=	GRCh37
NC_000002.10:g.31607897C=	NCBI36
NG_008365.1:g.56649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.682G= MANE Select	ENSP00000477587.1:p.Ala228=
ENST00000622030.1:c.682G=	ENSP00000477587.1:p.Ala228=
NM_000348.3:c.682G=	NP_000339.2:p.Ala228=
XM_011533069.1:c.460G=	XP_011531371.1:p.Ala154=
XM_011533070.1:c.427G=	XP_011531372.1:p.Ala143=
XM_011533071.1:c.427G=	XP_011531373.1:p.Ala143=
XM_011533072.1:c.427G=	XP_011531374.1:p.Ala143=
XM_011533069.2:c.460G=	XP_011531371.1:p.Ala154=
XM_011533072.2:c.427G=	XP_011531374.1:p.Ala143=
NM_000348.4:c.682G= MANE Select	NP_000339.2:p.Ala228=