Canonical Allele Identifier: CA2760283938

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291484_6291485insACT , CM000666.2:g.6291484_6291485insACT	GRCh38
NC_000004.11:g.6293211_6293212insACT , CM000666.1:g.6293211_6293212insACT	GRCh37
NC_000004.10:g.6344112_6344113insACT	NCBI36
NG_011700.1:g.26635_26636insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+117_631+118insACT	ENSP00000507852.1:n.631+117_631+118insACT
ENST00000683395.1:c.608+130_608+131insACT
ENST00000684087.1:c.631+117_631+118insACT	ENSP00000506978.1:n.631+117_631+118insACT
ENST00000684700.1:c.*43_*44insACT	ENSP00000507806.1:n.*43_*44insACT
ENST00000506362.2:c.382+117_382+118insACT	ENSP00000424103.2:n.382+117_382+118insACT
ENST00000673642.1:c.430+117_430+118insACT	ENSP00000501242.1:n.430+117_430+118insACT
ENST00000673991.1:c.631+117_631+118insACT	ENSP00000501033.1:n.631+117_631+118insACT
ENST00000226760.5:c.631+117_631+118insACT MANE Select	ENSP00000226760.1:n.631+117_631+118insACT
ENST00000503569.5:c.631+117_631+118insACT	ENSP00000423337.1:n.631+117_631+118insACT
ENST00000506362.1:c.228+117_228+118insACT
ENST00000507765.1:n.816+117_816+118insACT
NM_001145853.1:c.631+117_631+118insACT	NP_001139325.1:n.631+117_631+118insACT
NM_006005.3:c.631+117_631+118insACT MANE Select	NP_005996.2:n.631+117_631+118insACT
XM_017008586.1:c.640+117_640+118insACT	XP_016864075.1:n.640+117_640+118insACT