Canonical Allele Identifier: CA917120421

Gene: WFS1

Linked Data

• dbSNP Id: rs56102017

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291031_6291032insGCATGGCGCA , CM000666.2:g.6291031_6291032insGCATGGCGCA	GRCh38
NC_000004.11:g.6292758_6292759insGCATGGCGCA , CM000666.1:g.6292758_6292759insGCATGGCGCA	GRCh37
NC_000004.10:g.6343659_6343660insGCATGGCGCA	NCBI36
NG_011700.1:g.26182_26183insGCATGGCGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.461-166_461-165insGCATGGCGCA	ENSP00000507852.1:n.461-166_461-165insGCATGGCGCA
ENST00000683395.1:c.451-166_451-165insGCATGGCGCA
ENST00000684087.1:c.461-166_461-165insGCATGGCGCA	ENSP00000506978.1:n.461-166_461-165insGCATGGCGCA
ENST00000684700.1:c.461-166_461-165insGCATGGCGCA	ENSP00000507806.1:n.461-166_461-165insGCATGGCGCA
ENST00000506362.2:c.212-166_212-165insGCATGGCGCA	ENSP00000424103.2:n.212-166_212-165insGCATGGCGCA
ENST00000673642.1:c.260-166_260-165insGCATGGCGCA	ENSP00000501242.1:n.260-166_260-165insGCATGGCGCA
ENST00000673991.1:c.461-166_461-165insGCATGGCGCA	ENSP00000501033.1:n.461-166_461-165insGCATGGCGCA
ENST00000674051.1:c.335-166_335-165insGCATGGCGCA	ENSP00000501083.1:n.335-166_335-165insGCATGGCGCA
ENST00000226760.5:c.461-166_461-165insGCATGGCGCA MANE Select	ENSP00000226760.1:n.461-166_461-165insGCATGGCGCA
ENST00000503569.5:c.461-166_461-165insGCATGGCGCA	ENSP00000423337.1:n.461-166_461-165insGCATGGCGCA
ENST00000506362.1:c.58-166_58-165insGCATGGCGCA
ENST00000507765.1:n.646-166_646-165insGCATGGCGCA
NM_001145853.1:c.461-166_461-165insGCATGGCGCA	NP_001139325.1:n.461-166_461-165insGCATGGCGCA
NM_006005.3:c.461-166_461-165insGCATGGCGCA MANE Select	NP_005996.2:n.461-166_461-165insGCATGGCGCA
XM_017008586.1:c.470-166_470-165insGCATGGCGCA	XP_016864075.1:n.470-166_470-165insGCATGGCGCA