Canonical Allele Identifier: CA2669843455

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301662-ATGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301665_6301667del , CM000666.2:g.6301665_6301667del	GRCh38
NC_000004.11:g.6303392_6303394del , CM000666.1:g.6303392_6303394del	GRCh37
NC_000004.10:g.6354293_6354295del	NCBI36
NG_011700.1:g.36816_36818del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1906_1908del	ENSP00000507852.1:p.Val636del
ENST00000683395.1:c.1847_1849del
ENST00000684087.1:c.1870_1872del	ENSP00000506978.1:p.Val624del
ENST00000506362.2:c.1621_1623del	ENSP00000424103.2:p.Val541del
ENST00000673642.1:c.1529_1531del	ENSP00000501242.1:n.1529_1531del
ENST00000673991.1:c.1906_1908del	ENSP00000501033.1:p.Val636del
ENST00000226760.5:c.1870_1872del MANE Select	ENSP00000226760.1:p.Val624del
ENST00000503569.5:c.1870_1872del	ENSP00000423337.1:p.Val624del
ENST00000507765.1:n.2055_2057del
NM_001145853.1:c.1870_1872del	NP_001139325.1:p.Val624del
NM_006005.3:c.1870_1872del MANE Select	NP_005996.2:p.Val624del
XM_017008586.1:c.1879_1881del	XP_016864075.1:p.Val627del