Canonical Allele Identifier: CA1242215055

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31568314G= , CM000664.2:g.31568314G=	GRCh38
NC_000002.11:g.31793384G= , CM000664.1:g.31793384G=	GRCh37
NC_000002.10:g.31646888G=	NCBI36
NG_008365.1:g.17658C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+12306C= MANE Select	ENSP00000477587.1:n.281+12306C=
ENST00000622030.1:c.281+12306C=	ENSP00000477587.1:n.281+12306C=
NM_000348.3:c.281+12306C=	NP_000339.2:n.281+12306C=
XM_011533068.1:c.281+12306C=	XP_011531370.1:n.281+12306C=
XM_011533070.1:c.27-34548C=	XP_011531372.1:n.27-34548C=
XM_011533071.1:c.27-34548C=	XP_011531373.1:n.27-34548C=
XM_011533072.1:c.27-34548C=	XP_011531374.1:n.27-34548C=
XM_011533072.2:c.27-34548C=	XP_011531374.1:n.27-34548C=
NM_000348.4:c.281+12306C= MANE Select	NP_000339.2:n.281+12306C=