Canonical Allele Identifier: CA2760284009

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291519_6291520insAGA , CM000666.2:g.6291519_6291520insAGA	GRCh38
NC_000004.11:g.6293246_6293247insAGA , CM000666.1:g.6293246_6293247insAGA	GRCh37
NC_000004.10:g.6344147_6344148insAGA	NCBI36
NG_011700.1:g.26670_26671insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+152_631+153insAGA	ENSP00000507852.1:n.631+152_631+153insAGA
ENST00000683395.1:c.608+165_608+166insAGA
ENST00000684087.1:c.631+152_631+153insAGA	ENSP00000506978.1:n.631+152_631+153insAGA
ENST00000684700.1:c.*78_*79insAGA	ENSP00000507806.1:n.*78_*79insAGA
ENST00000506362.2:c.382+152_382+153insAGA	ENSP00000424103.2:n.382+152_382+153insAGA
ENST00000673642.1:c.430+152_430+153insAGA	ENSP00000501242.1:n.430+152_430+153insAGA
ENST00000673991.1:c.631+152_631+153insAGA	ENSP00000501033.1:n.631+152_631+153insAGA
ENST00000226760.5:c.631+152_631+153insAGA MANE Select	ENSP00000226760.1:n.631+152_631+153insAGA
ENST00000503569.5:c.631+152_631+153insAGA	ENSP00000423337.1:n.631+152_631+153insAGA
ENST00000506362.1:c.228+152_228+153insAGA
ENST00000507765.1:n.816+152_816+153insAGA
NM_001145853.1:c.631+152_631+153insAGA	NP_001139325.1:n.631+152_631+153insAGA
NM_006005.3:c.631+152_631+153insAGA MANE Select	NP_005996.2:n.631+152_631+153insAGA
XM_017008586.1:c.640+152_640+153insAGA	XP_016864075.1:n.640+152_640+153insAGA