Canonical Allele Identifier: CA1525226530

Gene: SRD5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6651866G= , CM000667.2:g.6651866G=	GRCh38
NC_000005.9:g.6651979G= , CM000667.1:g.6651979G=	GRCh37
NC_000005.8:g.6704979G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504286.2:c.318G=	ENSP00000518753.1:p.Met106=
ENST00000510531.6:c.*439G=	ENSP00000425330.1:n.*439G=
ENST00000274192.7:c.318G= MANE Select	ENSP00000274192.5:p.Met106=
ENST00000274192.6:c.318G=	ENSP00000274192.5:p.Met106=
ENST00000504286.1:n.439G=
ENST00000510531.5:c.*439G=	ENSP00000425330.1:n.*439G=
ENST00000513117.1:c.294-4212G=	ENSP00000421342.1:n.294-4212G=
NM_001047.2:c.318G=	NP_001038.1:p.Met106=
XM_011514103.1:c.320-4212G=	XP_011512405.1:n.320-4212G=
NM_001047.3:c.318G=	NP_001038.1:p.Met106=
NM_001324322.1:c.320-4212G=	NP_001311251.1:n.320-4212G=
NM_001324323.1:c.99G=	NP_001311252.1:p.Met33=
NR_136739.1:n.573G=
NM_001047.4:c.318G= MANE Select	NP_001038.1:p.Met106=
NM_001324322.2:c.320-4212G=	NP_001311251.1:n.320-4212G=
NM_001324323.2:c.99G=	NP_001311252.1:p.Met33=
NR_136739.2:n.455G=