Canonical Allele Identifier: CA1242214523

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567239C= , CM000664.2:g.31567239C=	GRCh38
NC_000002.11:g.31792309C= , CM000664.1:g.31792309C=	GRCh37
NC_000002.10:g.31645813C=	NCBI36
NG_008365.1:g.18733G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13381G= MANE Select	ENSP00000477587.1:n.281+13381G=
ENST00000622030.1:c.281+13381G=	ENSP00000477587.1:n.281+13381G=
NM_000348.3:c.281+13381G=	NP_000339.2:n.281+13381G=
XM_011533068.1:c.281+13381G=	XP_011531370.1:n.281+13381G=
XM_011533070.1:c.27-33473G=	XP_011531372.1:n.27-33473G=
XM_011533071.1:c.27-33473G=	XP_011531373.1:n.27-33473G=
XM_011533072.1:c.27-33473G=	XP_011531374.1:n.27-33473G=
XM_011533072.2:c.27-33473G=	XP_011531374.1:n.27-33473G=
NM_000348.4:c.281+13381G= MANE Select	NP_000339.2:n.281+13381G=