Canonical Allele Identifier: CA2760284102

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291566_6291567insACT , CM000666.2:g.6291566_6291567insACT	GRCh38
NC_000004.11:g.6293293_6293294insACT , CM000666.1:g.6293293_6293294insACT	GRCh37
NC_000004.10:g.6344194_6344195insACT	NCBI36
NG_011700.1:g.26717_26718insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+199_631+200insACT	ENSP00000507852.1:n.631+199_631+200insACT
ENST00000683395.1:c.608+212_608+213insACT
ENST00000684087.1:c.631+199_631+200insACT	ENSP00000506978.1:n.631+199_631+200insACT
ENST00000684700.1:c.*125_*126insACT	ENSP00000507806.1:n.*125_*126insACT
ENST00000506362.2:c.382+199_382+200insACT	ENSP00000424103.2:n.382+199_382+200insACT
ENST00000673642.1:c.430+199_430+200insACT	ENSP00000501242.1:n.430+199_430+200insACT
ENST00000673991.1:c.631+199_631+200insACT	ENSP00000501033.1:n.631+199_631+200insACT
ENST00000226760.5:c.631+199_631+200insACT MANE Select	ENSP00000226760.1:n.631+199_631+200insACT
ENST00000503569.5:c.631+199_631+200insACT	ENSP00000423337.1:n.631+199_631+200insACT
ENST00000506362.1:c.228+199_228+200insACT
ENST00000507765.1:n.816+199_816+200insACT
NM_001145853.1:c.631+199_631+200insACT	NP_001139325.1:n.631+199_631+200insACT
NM_006005.3:c.631+199_631+200insACT MANE Select	NP_005996.2:n.631+199_631+200insACT
XM_017008586.1:c.640+199_640+200insACT	XP_016864075.1:n.640+199_640+200insACT