Canonical Allele Identifier: CA1242198314

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531398C= , CM000664.2:g.31531398C=	GRCh38
NC_000002.11:g.31756468C= , CM000664.1:g.31756468C=	GRCh37
NC_000002.10:g.31609972C=	NCBI36
NG_008365.1:g.54574G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.520G= MANE Select	ENSP00000477587.1:p.Gly174=
ENST00000622030.1:c.520G=	ENSP00000477587.1:p.Gly174=
NM_000348.3:c.520G=	NP_000339.2:p.Gly174=
XM_011533069.1:c.298G=	XP_011531371.1:p.Gly100=
XM_011533070.1:c.265G=	XP_011531372.1:p.Gly89=
XM_011533071.1:c.265G=	XP_011531373.1:p.Gly89=
XM_011533072.1:c.265G=	XP_011531374.1:p.Gly89=
XM_011533069.2:c.298G=	XP_011531371.1:p.Gly100=
XM_011533072.2:c.265G=	XP_011531374.1:p.Gly89=
NM_000348.4:c.520G= MANE Select	NP_000339.2:p.Gly174=