Canonical Allele Identifier: CA1242197411

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529407C= , CM000664.2:g.31529407C=	GRCh38
NC_000002.11:g.31754477C= , CM000664.1:g.31754477C=	GRCh37
NC_000002.10:g.31607981C=	NCBI36
NG_008365.1:g.56565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.598G= MANE Select	ENSP00000477587.1:p.Glu200=
ENST00000622030.1:c.598G=	ENSP00000477587.1:p.Glu200=
NM_000348.3:c.598G=	NP_000339.2:p.Glu200=
XM_011533069.1:c.376G=	XP_011531371.1:p.Glu126=
XM_011533070.1:c.343G=	XP_011531372.1:p.Glu115=
XM_011533071.1:c.343G=	XP_011531373.1:p.Glu115=
XM_011533072.1:c.343G=	XP_011531374.1:p.Glu115=
XM_011533069.2:c.376G=	XP_011531371.1:p.Glu126=
XM_011533072.2:c.343G=	XP_011531374.1:p.Glu115=
NM_000348.4:c.598G= MANE Select	NP_000339.2:p.Glu200=