Canonical Allele Identifier: CA356178755
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1230104441
gnomAD v2: 4-6304026-G-A
gnomAD v3: 4-6302299-G-A
gnomAD v4: 4-6302299-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302299G>A , CM000666.2:g.6302299G>A GRCh38
NC_000004.11:g.6304026G>A , CM000666.1:g.6304026G>A GRCh37
NC_000004.10:g.6354927G>A NCBI36
NG_011700.1:g.37450G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2540G>A ENSP00000507852.1:p.Ser847Asn
ENST00000683395.1:c.2481G>A
ENST00000684087.1:c.2504G>A ENSP00000506978.1:p.Ser835Asn
ENST00000506362.2:c.2255G>A ENSP00000424103.2:p.Ser752Asn
ENST00000673991.1:c.2540G>A ENSP00000501033.1:p.Ser847Asn
ENST00000226760.5:c.2504G>A MANE Select ENSP00000226760.1:p.Ser835Asn
ENST00000503569.5:c.2504G>A ENSP00000423337.1:p.Ser835Asn
ENST00000507765.1:n.2689G>A
NM_001145853.1:c.2504G>A NP_001139325.1:p.Ser835Asn
NM_006005.3:c.2504G>A MANE Select NP_005996.2:p.Ser835Asn
XM_017008586.1:c.2513G>A XP_016864075.1:p.Ser838Asn