Canonical Allele Identifier: CA2669843458

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302096-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302100_6302102del , CM000666.2:g.6302100_6302102del	GRCh38
NC_000004.11:g.6303827_6303829del , CM000666.1:g.6303827_6303829del	GRCh37
NC_000004.10:g.6354728_6354730del	NCBI36
NG_011700.1:g.37251_37253del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2341_2343del	ENSP00000507852.1:p.Lys781del
ENST00000683395.1:c.2282_2284del
ENST00000684087.1:c.2305_2307del	ENSP00000506978.1:p.Lys769del
ENST00000506362.2:c.2056_2058del	ENSP00000424103.2:p.Lys686del
ENST00000673642.1:c.1964_1966del	ENSP00000501242.1:n.1964_1966del
ENST00000673991.1:c.2341_2343del	ENSP00000501033.1:p.Lys781del
ENST00000226760.5:c.2305_2307del MANE Select	ENSP00000226760.1:p.Lys769del
ENST00000503569.5:c.2305_2307del	ENSP00000423337.1:p.Lys769del
ENST00000507765.1:n.2490_2492del
NM_001145853.1:c.2305_2307del	NP_001139325.1:p.Lys769del
NM_006005.3:c.2305_2307del MANE Select	NP_005996.2:p.Lys769del
XM_017008586.1:c.2314_2316del	XP_016864075.1:p.Lys772del