Canonical Allele Identifier: CA2760283948

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291489_6291490insGAT , CM000666.2:g.6291489_6291490insGAT	GRCh38
NC_000004.11:g.6293216_6293217insGAT , CM000666.1:g.6293216_6293217insGAT	GRCh37
NC_000004.10:g.6344117_6344118insGAT	NCBI36
NG_011700.1:g.26640_26641insGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+122_631+123insGAT	ENSP00000507852.1:n.631+122_631+123insGAT
ENST00000683395.1:c.608+135_608+136insGAT
ENST00000684087.1:c.631+122_631+123insGAT	ENSP00000506978.1:n.631+122_631+123insGAT
ENST00000684700.1:c.*48_*49insGAT	ENSP00000507806.1:n.*48_*49insGAT
ENST00000506362.2:c.382+122_382+123insGAT	ENSP00000424103.2:n.382+122_382+123insGAT
ENST00000673642.1:c.430+122_430+123insGAT	ENSP00000501242.1:n.430+122_430+123insGAT
ENST00000673991.1:c.631+122_631+123insGAT	ENSP00000501033.1:n.631+122_631+123insGAT
ENST00000226760.5:c.631+122_631+123insGAT MANE Select	ENSP00000226760.1:n.631+122_631+123insGAT
ENST00000503569.5:c.631+122_631+123insGAT	ENSP00000423337.1:n.631+122_631+123insGAT
ENST00000506362.1:c.228+122_228+123insGAT
ENST00000507765.1:n.816+122_816+123insGAT
NM_001145853.1:c.631+122_631+123insGAT	NP_001139325.1:n.631+122_631+123insGAT
NM_006005.3:c.631+122_631+123insGAT MANE Select	NP_005996.2:n.631+122_631+123insGAT
XM_017008586.1:c.640+122_640+123insGAT	XP_016864075.1:n.640+122_640+123insGAT