Canonical Allele Identifier: CA2669825778

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291114-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291116del , CM000666.2:g.6291116del	GRCh38
NC_000004.11:g.6292843del , CM000666.1:g.6292843del	GRCh37
NC_000004.10:g.6343744del	NCBI36
NG_011700.1:g.26267del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.461-81del	ENSP00000507852.1:n.461-81del
ENST00000683395.1:c.451-81del
ENST00000684087.1:c.461-81del	ENSP00000506978.1:n.461-81del
ENST00000684700.1:c.461-81del	ENSP00000507806.1:n.461-81del
ENST00000506362.2:c.212-81del	ENSP00000424103.2:n.212-81del
ENST00000673642.1:c.260-81del	ENSP00000501242.1:n.260-81del
ENST00000673991.1:c.461-81del	ENSP00000501033.1:n.461-81del
ENST00000674051.1:c.335-81del	ENSP00000501083.1:n.335-81del
ENST00000226760.5:c.461-81del MANE Select	ENSP00000226760.1:n.461-81del
ENST00000503569.5:c.461-81del	ENSP00000423337.1:n.461-81del
ENST00000506362.1:c.58-81del
ENST00000507765.1:n.646-81del
NM_001145853.1:c.461-81del	NP_001139325.1:n.461-81del
NM_006005.3:c.461-81del MANE Select	NP_005996.2:n.461-81del
XM_017008586.1:c.470-81del	XP_016864075.1:n.470-81del