Canonical Allele Identifier: CA2673164875

Gene: SRD5A1

Linked Data

• gnomAD v4: 5-6651783-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6651783T>C , CM000667.2:g.6651783T>C	GRCh38
NC_000005.9:g.6651896T>C , CM000667.1:g.6651896T>C	GRCh37
NC_000005.8:g.6704896T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504286.2:c.294-59T>C	ENSP00000518753.1:n.294-59T>C
ENST00000510531.6:c.*415-59T>C	ENSP00000425330.1:n.*415-59T>C
ENST00000274192.7:c.294-59T>C MANE Select	ENSP00000274192.5:n.294-59T>C
ENST00000274192.6:c.294-59T>C	ENSP00000274192.5:n.294-59T>C
ENST00000504286.1:n.415-59T>C
ENST00000510531.5:c.*415-59T>C	ENSP00000425330.1:n.*415-59T>C
ENST00000513117.1:c.294-4295T>C	ENSP00000421342.1:n.294-4295T>C
NM_001047.2:c.294-59T>C	NP_001038.1:n.294-59T>C
XM_011514103.1:c.320-4295T>C	XP_011512405.1:n.320-4295T>C
NM_001047.3:c.294-59T>C	NP_001038.1:n.294-59T>C
NM_001324322.1:c.320-4295T>C	NP_001311251.1:n.320-4295T>C
NM_001324323.1:c.75-59T>C	NP_001311252.1:n.75-59T>C
NR_136739.1:n.549-59T>C
NM_001047.4:c.294-59T>C MANE Select	NP_001038.1:n.294-59T>C
NM_001324322.2:c.320-4295T>C	NP_001311251.1:n.320-4295T>C
NM_001324323.2:c.75-59T>C	NP_001311252.1:n.75-59T>C
NR_136739.2:n.431-59T>C