Canonical Allele Identifier: CA359134623

Gene: SRD5A1

Linked Data

• dbSNP Id: rs1423767939
• gnomAD v4: 5-6651864-A-G
• MyVariant Identifiers: chr5:g.6651977A>G (hg19) ; chr5:g.6651864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6651864A>G , CM000667.2:g.6651864A>G	GRCh38
NC_000005.9:g.6651977A>G , CM000667.1:g.6651977A>G	GRCh37
NC_000005.8:g.6704977A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504286.2:c.316A>G	ENSP00000518753.1:p.Met106Val
ENST00000510531.6:c.*437A>G	ENSP00000425330.1:n.*437A>G
ENST00000274192.7:c.316A>G MANE Select	ENSP00000274192.5:p.Met106Val
ENST00000274192.6:c.316A>G	ENSP00000274192.5:p.Met106Val
ENST00000504286.1:n.437A>G
ENST00000510531.5:c.*437A>G	ENSP00000425330.1:n.*437A>G
ENST00000513117.1:c.294-4214A>G	ENSP00000421342.1:n.294-4214A>G
NM_001047.2:c.316A>G	NP_001038.1:p.Met106Val
XM_011514103.1:c.320-4214A>G	XP_011512405.1:n.320-4214A>G
NM_001047.3:c.316A>G	NP_001038.1:p.Met106Val
NM_001324322.1:c.320-4214A>G	NP_001311251.1:n.320-4214A>G
NM_001324323.1:c.97A>G	NP_001311252.1:p.Met33Val
NR_136739.1:n.571A>G
NM_001047.4:c.316A>G MANE Select	NP_001038.1:p.Met106Val
NM_001324322.2:c.320-4214A>G	NP_001311251.1:n.320-4214A>G
NM_001324323.2:c.97A>G	NP_001311252.1:p.Met33Val
NR_136739.2:n.453A>G