Canonical Allele Identifier: CA1525250675

Gene: SRD5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6661853C= , CM000667.2:g.6661853C=	GRCh38
NC_000005.9:g.6661966C= , CM000667.1:g.6661966C=	GRCh37
NC_000005.8:g.6714966C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001047.4:c.563-963C= MANE Select	NP_001038.1:n.563-963C=
ENST00000274192.7:c.563-963C= MANE Select	ENSP00000274192.5:n.563-963C=
NM_001047.2:c.563-963C=	NP_001038.1:n.563-963C=
NM_001047.3:c.563-963C=	NP_001038.1:n.563-963C=
NM_001324322.1:c.422-963C=	NP_001311251.1:n.422-963C=
NM_001324322.2:c.422-963C=	NP_001311251.1:n.422-963C=
NM_001324323.1:c.344-963C=	NP_001311252.1:n.344-963C=
NM_001324323.2:c.344-963C=	NP_001311252.1:n.344-963C=
NR_136739.1:n.1008-963C=
NR_136739.2:n.890-963C=
ENST00000274192.6:c.563-963C=	ENSP00000274192.5:n.563-963C=
ENST00000504286.2:c.753-963C=	ENSP00000518753.1:n.753-963C=
ENST00000510531.5:c.*684-963C=	ENSP00000425330.1:n.*684-963C=
ENST00000510531.6:c.*684-963C=	ENSP00000425330.1:n.*684-963C=
ENST00000513117.1:c.396-963C=	ENSP00000421342.1:n.396-963C=
XM_011514103.1:c.422-963C=	XP_011512405.1:n.422-963C=