Canonical Allele Identifier: CA2669825010

Gene: WFS1

Linked Data

• gnomAD v4: 4-6277697-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6277697C>A , CM000666.2:g.6277697C>A	GRCh38
NC_000004.11:g.6279424C>A , CM000666.1:g.6279424C>A	GRCh37
NC_000004.10:g.6330325C>A	NCBI36
NG_011700.1:g.12848C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506588.6:n.402+10C>A
ENST00000682059.1:c.232+10C>A	ENSP00000507988.1:n.232+10C>A
ENST00000682275.1:c.232+10C>A	ENSP00000507852.1:n.232+10C>A
ENST00000683395.1:c.222+10C>A
ENST00000684054.1:c.232+10C>A	ENSP00000507120.1:n.232+10C>A
ENST00000684087.1:c.232+10C>A	ENSP00000506978.1:n.232+10C>A
ENST00000684700.1:c.232+10C>A	ENSP00000507806.1:n.232+10C>A
ENST00000506362.2:c.-18+7683C>A	ENSP00000424103.2:n.-18+7683C>A
ENST00000673642.1:c.31+10C>A	ENSP00000501242.1:n.31+10C>A
ENST00000673991.1:c.232+10C>A	ENSP00000501033.1:n.232+10C>A
ENST00000674051.1:c.106+10C>A	ENSP00000501083.1:n.106+10C>A
ENST00000226760.5:c.232+10C>A MANE Select	ENSP00000226760.1:n.232+10C>A
ENST00000503569.5:c.232+10C>A	ENSP00000423337.1:n.232+10C>A
ENST00000506588.5:n.402+10C>A
NM_001145853.1:c.232+10C>A	NP_001139325.1:n.232+10C>A
NM_006005.3:c.232+10C>A MANE Select	NP_005996.2:n.232+10C>A
XM_017008586.1:c.241+10C>A	XP_016864075.1:n.241+10C>A