Canonical Allele Identifier: CA1242195960

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526257T= , CM000664.2:g.31526257T=	GRCh38
NC_000002.11:g.31751327T= , CM000664.1:g.31751327T=	GRCh37
NC_000002.10:g.31604831T=	NCBI36
NG_008365.1:g.59715A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.704A= MANE Select	ENSP00000477587.1:p.Tyr235=
ENST00000622030.1:c.704A=	ENSP00000477587.1:p.Tyr235=
NM_000348.3:c.704A=	NP_000339.2:p.Tyr235=
XM_011533069.1:c.482A=	XP_011531371.1:p.Tyr161=
XM_011533070.1:c.449A=	XP_011531372.1:p.Tyr150=
XM_011533071.1:c.449A=	XP_011531373.1:p.Tyr150=
XM_011533072.1:c.449A=	XP_011531374.1:p.Tyr150=
XM_011533069.2:c.482A=	XP_011531371.1:p.Tyr161=
XM_011533072.2:c.449A=	XP_011531374.1:p.Tyr150=
NM_000348.4:c.704A= MANE Select	NP_000339.2:p.Tyr235=