Canonical Allele Identifier: CA1242197424

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529432T= , CM000664.2:g.31529432T=	GRCh38
NC_000002.11:g.31754502T= , CM000664.1:g.31754502T=	GRCh37
NC_000002.10:g.31608006T=	NCBI36
NG_008365.1:g.56540A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.573A= MANE Select	ENSP00000477587.1:p.Gly191=
ENST00000622030.1:c.573A=	ENSP00000477587.1:p.Gly191=
NM_000348.3:c.573A=	NP_000339.2:p.Gly191=
XM_011533069.1:c.351A=	XP_011531371.1:p.Gly117=
XM_011533070.1:c.318A=	XP_011531372.1:p.Gly106=
XM_011533071.1:c.318A=	XP_011531373.1:p.Gly106=
XM_011533072.1:c.318A=	XP_011531374.1:p.Gly106=
XM_011533069.2:c.351A=	XP_011531371.1:p.Gly117=
XM_011533072.2:c.318A=	XP_011531374.1:p.Gly106=
NM_000348.4:c.573A= MANE Select	NP_000339.2:p.Gly191=