Canonical Allele Identifier: CA113771967

Gene: SRD5A1

Linked Data

• dbSNP Id: rs955586868
• gnomAD v2: 5-6651563-A-T
• gnomAD v3: 5-6651450-A-T
• gnomAD v4: 5-6651450-A-T
• MyVariant Identifiers: chr5:g.6651563A>T (hg19) ; chr5:g.6651450A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6651450A>T , CM000667.2:g.6651450A>T	GRCh38
NC_000005.9:g.6651563A>T , CM000667.1:g.6651563A>T	GRCh37
NC_000005.8:g.6704563A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504286.2:c.294-392A>T	ENSP00000518753.1:n.294-392A>T
ENST00000510531.6:c.*415-392A>T	ENSP00000425330.1:n.*415-392A>T
ENST00000274192.7:c.294-392A>T MANE Select	ENSP00000274192.5:n.294-392A>T
ENST00000274192.6:c.294-392A>T	ENSP00000274192.5:n.294-392A>T
ENST00000504286.1:n.415-392A>T
ENST00000510531.5:c.*415-392A>T	ENSP00000425330.1:n.*415-392A>T
ENST00000513117.1:c.294-4628A>T	ENSP00000421342.1:n.294-4628A>T
NM_001047.2:c.294-392A>T	NP_001038.1:n.294-392A>T
XM_011514103.1:c.320-4628A>T	XP_011512405.1:n.320-4628A>T
NM_001047.3:c.294-392A>T	NP_001038.1:n.294-392A>T
NM_001324322.1:c.320-4628A>T	NP_001311251.1:n.320-4628A>T
NM_001324323.1:c.75-392A>T	NP_001311252.1:n.75-392A>T
NR_136739.1:n.549-392A>T
NM_001047.4:c.294-392A>T MANE Select	NP_001038.1:n.294-392A>T
NM_001324322.2:c.320-4628A>T	NP_001311251.1:n.320-4628A>T
NM_001324323.2:c.75-392A>T	NP_001311252.1:n.75-392A>T
NR_136739.2:n.431-392A>T