Canonical Allele Identifier: CA1242214644

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567465T= , CM000664.2:g.31567465T=	GRCh38
NC_000002.11:g.31792535T= , CM000664.1:g.31792535T=	GRCh37
NC_000002.10:g.31646039T=	NCBI36
NG_008365.1:g.18507A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13155A= MANE Select	ENSP00000477587.1:n.281+13155A=
ENST00000622030.1:c.281+13155A=	ENSP00000477587.1:n.281+13155A=
NM_000348.3:c.281+13155A=	NP_000339.2:n.281+13155A=
XM_011533068.1:c.281+13155A=	XP_011531370.1:n.281+13155A=
XM_011533070.1:c.27-33699A=	XP_011531372.1:n.27-33699A=
XM_011533071.1:c.27-33699A=	XP_011531373.1:n.27-33699A=
XM_011533072.1:c.27-33699A=	XP_011531374.1:n.27-33699A=
XM_011533072.2:c.27-33699A=	XP_011531374.1:n.27-33699A=
NM_000348.4:c.281+13155A= MANE Select	NP_000339.2:n.281+13155A=