Canonical Allele Identifier: CA2760283795

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6290987_6290994del , CM000666.2:g.6290987_6290994del	GRCh38
NC_000004.11:g.6292714_6292721del , CM000666.1:g.6292714_6292721del	GRCh37
NC_000004.10:g.6343615_6343622del	NCBI36
NG_011700.1:g.26138_26145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.461-210_461-203del	ENSP00000507852.1:n.461-210_461-203del
ENST00000683395.1:c.451-210_451-203del
ENST00000684087.1:c.461-210_461-203del	ENSP00000506978.1:n.461-210_461-203del
ENST00000684700.1:c.461-210_461-203del	ENSP00000507806.1:n.461-210_461-203del
ENST00000506362.2:c.212-210_212-203del	ENSP00000424103.2:n.212-210_212-203del
ENST00000673642.1:c.260-210_260-203del	ENSP00000501242.1:n.260-210_260-203del
ENST00000673991.1:c.461-210_461-203del	ENSP00000501033.1:n.461-210_461-203del
ENST00000674051.1:c.335-210_335-203del	ENSP00000501083.1:n.335-210_335-203del
ENST00000226760.5:c.461-210_461-203del MANE Select	ENSP00000226760.1:n.461-210_461-203del
ENST00000503569.5:c.461-210_461-203del	ENSP00000423337.1:n.461-210_461-203del
ENST00000506362.1:c.58-210_58-203del
ENST00000507765.1:n.646-210_646-203del
NM_001145853.1:c.461-210_461-203del	NP_001139325.1:n.461-210_461-203del
NM_006005.3:c.461-210_461-203del MANE Select	NP_005996.2:n.461-210_461-203del
XM_017008586.1:c.470-210_470-203del	XP_016864075.1:n.470-210_470-203del