Canonical Allele Identifier: CA2760284000

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291513_6291514insAGA , CM000666.2:g.6291513_6291514insAGA	GRCh38
NC_000004.11:g.6293240_6293241insAGA , CM000666.1:g.6293240_6293241insAGA	GRCh37
NC_000004.10:g.6344141_6344142insAGA	NCBI36
NG_011700.1:g.26664_26665insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+146_631+147insAGA	ENSP00000507852.1:n.631+146_631+147insAGA
ENST00000683395.1:c.608+159_608+160insAGA
ENST00000684087.1:c.631+146_631+147insAGA	ENSP00000506978.1:n.631+146_631+147insAGA
ENST00000684700.1:c.*72_*73insAGA	ENSP00000507806.1:n.*72_*73insAGA
ENST00000506362.2:c.382+146_382+147insAGA	ENSP00000424103.2:n.382+146_382+147insAGA
ENST00000673642.1:c.430+146_430+147insAGA	ENSP00000501242.1:n.430+146_430+147insAGA
ENST00000673991.1:c.631+146_631+147insAGA	ENSP00000501033.1:n.631+146_631+147insAGA
ENST00000226760.5:c.631+146_631+147insAGA MANE Select	ENSP00000226760.1:n.631+146_631+147insAGA
ENST00000503569.5:c.631+146_631+147insAGA	ENSP00000423337.1:n.631+146_631+147insAGA
ENST00000506362.1:c.228+146_228+147insAGA
ENST00000507765.1:n.816+146_816+147insAGA
NM_001145853.1:c.631+146_631+147insAGA	NP_001139325.1:n.631+146_631+147insAGA
NM_006005.3:c.631+146_631+147insAGA MANE Select	NP_005996.2:n.631+146_631+147insAGA
XM_017008586.1:c.640+146_640+147insAGA	XP_016864075.1:n.640+146_640+147insAGA