Canonical Allele Identifier: CA2669825992

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291400-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291400C>A , CM000666.2:g.6291400C>A	GRCh38
NC_000004.11:g.6293127C>A , CM000666.1:g.6293127C>A	GRCh37
NC_000004.10:g.6344028C>A	NCBI36
NG_011700.1:g.26551C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+33C>A	ENSP00000507852.1:n.631+33C>A
ENST00000683395.1:c.608+46C>A
ENST00000684087.1:c.631+33C>A	ENSP00000506978.1:n.631+33C>A
ENST00000684700.1:c.664C>A	ENSP00000507806.1:p.Leu222Met
ENST00000506362.2:c.382+33C>A	ENSP00000424103.2:n.382+33C>A
ENST00000673642.1:c.430+33C>A	ENSP00000501242.1:n.430+33C>A
ENST00000673991.1:c.631+33C>A	ENSP00000501033.1:n.631+33C>A
ENST00000226760.5:c.631+33C>A MANE Select	ENSP00000226760.1:n.631+33C>A
ENST00000503569.5:c.631+33C>A	ENSP00000423337.1:n.631+33C>A
ENST00000506362.1:c.228+33C>A
ENST00000507765.1:n.816+33C>A
NM_001145853.1:c.631+33C>A	NP_001139325.1:n.631+33C>A
NM_006005.3:c.631+33C>A MANE Select	NP_005996.2:n.631+33C>A
XM_017008586.1:c.640+33C>A	XP_016864075.1:n.640+33C>A