Canonical Allele Identifier: CA2760284082

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291555_6291556insAGA , CM000666.2:g.6291555_6291556insAGA	GRCh38
NC_000004.11:g.6293282_6293283insAGA , CM000666.1:g.6293282_6293283insAGA	GRCh37
NC_000004.10:g.6344183_6344184insAGA	NCBI36
NG_011700.1:g.26706_26707insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+188_631+189insAGA	ENSP00000507852.1:n.631+188_631+189insAGA
ENST00000683395.1:c.608+201_608+202insAGA
ENST00000684087.1:c.631+188_631+189insAGA	ENSP00000506978.1:n.631+188_631+189insAGA
ENST00000684700.1:c.*114_*115insAGA	ENSP00000507806.1:n.*114_*115insAGA
ENST00000506362.2:c.382+188_382+189insAGA	ENSP00000424103.2:n.382+188_382+189insAGA
ENST00000673642.1:c.430+188_430+189insAGA	ENSP00000501242.1:n.430+188_430+189insAGA
ENST00000673991.1:c.631+188_631+189insAGA	ENSP00000501033.1:n.631+188_631+189insAGA
ENST00000226760.5:c.631+188_631+189insAGA MANE Select	ENSP00000226760.1:n.631+188_631+189insAGA
ENST00000503569.5:c.631+188_631+189insAGA	ENSP00000423337.1:n.631+188_631+189insAGA
ENST00000506362.1:c.228+188_228+189insAGA
ENST00000507765.1:n.816+188_816+189insAGA
NM_001145853.1:c.631+188_631+189insAGA	NP_001139325.1:n.631+188_631+189insAGA
NM_006005.3:c.631+188_631+189insAGA MANE Select	NP_005996.2:n.631+188_631+189insAGA
XM_017008586.1:c.640+188_640+189insAGA	XP_016864075.1:n.640+188_640+189insAGA