Canonical Allele Identifier: CA2669825838

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291181-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291181_6291182insT , CM000666.2:g.6291181_6291182insT	GRCh38
NC_000004.11:g.6292908_6292909insT , CM000666.1:g.6292908_6292909insT	GRCh37
NC_000004.10:g.6343809_6343810insT	NCBI36
NG_011700.1:g.26332_26333insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.461-16_461-15insT	ENSP00000507852.1:n.461-16_461-15insT
ENST00000683395.1:c.451-16_451-15insT
ENST00000684087.1:c.461-16_461-15insT	ENSP00000506978.1:n.461-16_461-15insT
ENST00000684700.1:c.461-16_461-15insT	ENSP00000507806.1:n.461-16_461-15insT
ENST00000506362.2:c.212-16_212-15insT	ENSP00000424103.2:n.212-16_212-15insT
ENST00000673642.1:c.260-16_260-15insT	ENSP00000501242.1:n.260-16_260-15insT
ENST00000673991.1:c.461-16_461-15insT	ENSP00000501033.1:n.461-16_461-15insT
ENST00000674051.1:c.335-16_335-15insT	ENSP00000501083.1:n.335-16_335-15insT
ENST00000226760.5:c.461-16_461-15insT MANE Select	ENSP00000226760.1:n.461-16_461-15insT
ENST00000503569.5:c.461-16_461-15insT	ENSP00000423337.1:n.461-16_461-15insT
ENST00000506362.1:c.58-16_58-15insT
ENST00000507765.1:n.646-16_646-15insT
NM_001145853.1:c.461-16_461-15insT	NP_001139325.1:n.461-16_461-15insT
NM_006005.3:c.461-16_461-15insT MANE Select	NP_005996.2:n.461-16_461-15insT
XM_017008586.1:c.470-16_470-15insT	XP_016864075.1:n.470-16_470-15insT