Canonical Allele Identifier: CA2669826108

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291514-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291514T>A , CM000666.2:g.6291514T>A	GRCh38
NC_000004.11:g.6293241T>A , CM000666.1:g.6293241T>A	GRCh37
NC_000004.10:g.6344142T>A	NCBI36
NG_011700.1:g.26665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+147T>A	ENSP00000507852.1:n.631+147T>A
ENST00000683395.1:c.608+160T>A
ENST00000684087.1:c.631+147T>A	ENSP00000506978.1:n.631+147T>A
ENST00000684700.1:c.*73T>A	ENSP00000507806.1:n.*73T>A
ENST00000506362.2:c.382+147T>A	ENSP00000424103.2:n.382+147T>A
ENST00000673642.1:c.430+147T>A	ENSP00000501242.1:n.430+147T>A
ENST00000673991.1:c.631+147T>A	ENSP00000501033.1:n.631+147T>A
ENST00000226760.5:c.631+147T>A MANE Select	ENSP00000226760.1:n.631+147T>A
ENST00000503569.5:c.631+147T>A	ENSP00000423337.1:n.631+147T>A
ENST00000506362.1:c.228+147T>A
ENST00000507765.1:n.816+147T>A
NM_001145853.1:c.631+147T>A	NP_001139325.1:n.631+147T>A
NM_006005.3:c.631+147T>A MANE Select	NP_005996.2:n.631+147T>A
XM_017008586.1:c.640+147T>A	XP_016864075.1:n.640+147T>A