Canonical Allele Identifier: CA3085660851

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526208T= , CM000664.2:g.31526208T=	GRCh38
NC_000002.11:g.31751278T= , CM000664.1:g.31751278T=	GRCh37
NC_000002.10:g.31604782T=	NCBI36
NG_008365.1:g.59764A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000348.4:c.753A= MANE Select	NP_000339.2:p.Pro251=
ENST00000622030.2:c.753A= MANE Select	ENSP00000477587.1:p.Pro251=
NM_000348.3:c.753A=	NP_000339.2:p.Pro251=
ENST00000622030.1:c.753A=	ENSP00000477587.1:p.Pro251=
XM_011533069.1:c.531A=	XP_011531371.1:p.Pro177=
XM_011533069.2:c.531A=	XP_011531371.1:p.Pro177=
XM_011533070.1:c.498A=	XP_011531372.1:p.Pro166=
XM_011533071.1:c.498A=	XP_011531373.1:p.Pro166=
XM_011533072.1:c.498A=	XP_011531374.1:p.Pro166=
XM_011533072.2:c.498A=	XP_011531374.1:p.Pro166=