Canonical Allele Identifier: CA2760271254

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302820_6302821insAGA , CM000666.2:g.6302820_6302821insAGA	GRCh38
NC_000004.11:g.6304547_6304548insAGA , CM000666.1:g.6304547_6304548insAGA	GRCh37
NC_000004.10:g.6355448_6355449insAGA	NCBI36
NG_011700.1:g.37971_37972insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*352_*353insAGA	ENSP00000507852.1:n.*352_*353insAGA
ENST00000683395.1:c.3002_3003insAGA
ENST00000684087.1:c.*352_*353insAGA	ENSP00000506978.1:n.*352_*353insAGA
ENST00000506362.2:c.*352_*353insAGA	ENSP00000424103.2:n.*352_*353insAGA
ENST00000673991.1:c.*352_*353insAGA	ENSP00000501033.1:n.*352_*353insAGA
ENST00000226760.5:c.*352_*353insAGA MANE Select	ENSP00000226760.1:n.*352_*353insAGA
ENST00000503569.5:c.*352_*353insAGA	ENSP00000423337.1:n.*352_*353insAGA
ENST00000507765.1:n.3210_3211insAGA
NM_001145853.1:c.*352_*353insAGA	NP_001139325.1:n.*352_*353insAGA
NM_006005.3:c.*352_*353insAGA MANE Select	NP_005996.2:n.*352_*353insAGA
XM_017008586.1:c.*352_*353insAGA	XP_016864075.1:n.*352_*353insAGA