Canonical Allele Identifier: CA1242199316

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533627A= , CM000664.2:g.31533627A=	GRCh38
NC_000002.11:g.31758697A= , CM000664.1:g.31758697A=	GRCh37
NC_000002.10:g.31612201A=	NCBI36
NG_008365.1:g.52345T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.421T= MANE Select	ENSP00000477587.1:p.Tyr141=
ENST00000622030.1:c.421T=	ENSP00000477587.1:p.Tyr141=
NM_000348.3:c.421T=	NP_000339.2:p.Tyr141=
XM_011533068.1:c.421T=	XP_011531370.1:p.Tyr141=
XM_011533069.1:c.199T=	XP_011531371.1:p.Tyr67=
XM_011533070.1:c.166T=	XP_011531372.1:p.Tyr56=
XM_011533071.1:c.166T=	XP_011531373.1:p.Tyr56=
XM_011533072.1:c.166T=	XP_011531374.1:p.Tyr56=
XM_011533069.2:c.199T=	XP_011531371.1:p.Tyr67=
XM_011533072.2:c.166T=	XP_011531374.1:p.Tyr56=
NM_000348.4:c.421T= MANE Select	NP_000339.2:p.Tyr141=