Canonical Allele Identifier: CA1242197421

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529425A= , CM000664.2:g.31529425A=	GRCh38
NC_000002.11:g.31754495A= , CM000664.1:g.31754495A=	GRCh37
NC_000002.10:g.31607999A=	NCBI36
NG_008365.1:g.56547T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.580T= MANE Select	ENSP00000477587.1:p.Phe194=
ENST00000622030.1:c.580T=	ENSP00000477587.1:p.Phe194=
NM_000348.3:c.580T=	NP_000339.2:p.Phe194=
XM_011533069.1:c.358T=	XP_011531371.1:p.Phe120=
XM_011533070.1:c.325T=	XP_011531372.1:p.Phe109=
XM_011533071.1:c.325T=	XP_011531373.1:p.Phe109=
XM_011533072.1:c.325T=	XP_011531374.1:p.Phe109=
XM_011533069.2:c.358T=	XP_011531371.1:p.Phe120=
XM_011533072.2:c.325T=	XP_011531374.1:p.Phe109=
NM_000348.4:c.580T= MANE Select	NP_000339.2:p.Phe194=