Canonical Allele Identifier: CA1242197418

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529419C= , CM000664.2:g.31529419C=	GRCh38
NC_000002.11:g.31754489C= , CM000664.1:g.31754489C=	GRCh37
NC_000002.10:g.31607993C=	NCBI36
NG_008365.1:g.56553G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.586G= MANE Select	ENSP00000477587.1:p.Gly196=
ENST00000622030.1:c.586G=	ENSP00000477587.1:p.Gly196=
NM_000348.3:c.586G=	NP_000339.2:p.Gly196=
XM_011533069.1:c.364G=	XP_011531371.1:p.Gly122=
XM_011533070.1:c.331G=	XP_011531372.1:p.Gly111=
XM_011533071.1:c.331G=	XP_011531373.1:p.Gly111=
XM_011533072.1:c.331G=	XP_011531374.1:p.Gly111=
XM_011533069.2:c.364G=	XP_011531371.1:p.Gly122=
XM_011533072.2:c.331G=	XP_011531374.1:p.Gly111=
NM_000348.4:c.586G= MANE Select	NP_000339.2:p.Gly196=