Canonical Allele Identifier: CA2578035820

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301411-TGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301415_6301417del , CM000666.2:g.6301415_6301417del	GRCh38
NC_000004.11:g.6303142_6303144del , CM000666.1:g.6303142_6303144del	GRCh37
NC_000004.10:g.6354043_6354045del	NCBI36
NG_011700.1:g.36566_36568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1656_1658del	ENSP00000507852.1:p.Trp552del
ENST00000683395.1:c.1597_1599del
ENST00000684087.1:c.1620_1622del	ENSP00000506978.1:p.Trp540del
ENST00000506362.2:c.1371_1373del	ENSP00000424103.2:p.Trp457del
ENST00000673642.1:c.1279_1281del	ENSP00000501242.1:p.Val427del
ENST00000673991.1:c.1656_1658del	ENSP00000501033.1:p.Trp552del
ENST00000226760.5:c.1620_1622del MANE Select	ENSP00000226760.1:p.Trp540del
ENST00000503569.5:c.1620_1622del	ENSP00000423337.1:p.Trp540del
ENST00000507765.1:n.1805_1807del
NM_001145853.1:c.1620_1622del	NP_001139325.1:p.Trp540del
NM_006005.3:c.1620_1622del MANE Select	NP_005996.2:p.Trp540del
XM_017008586.1:c.1629_1631del	XP_016864075.1:p.Trp543del