Canonical Allele Identifier: CA2760284015

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291523_6291524insA , CM000666.2:g.6291523_6291524insA	GRCh38
NC_000004.11:g.6293250_6293251insA , CM000666.1:g.6293250_6293251insA	GRCh37
NC_000004.10:g.6344151_6344152insA	NCBI36
NG_011700.1:g.26674_26675insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+156_631+157insA	ENSP00000507852.1:n.631+156_631+157insA
ENST00000683395.1:c.608+169_608+170insA
ENST00000684087.1:c.631+156_631+157insA	ENSP00000506978.1:n.631+156_631+157insA
ENST00000684700.1:c.*82_*83insA	ENSP00000507806.1:n.*82_*83insA
ENST00000506362.2:c.382+156_382+157insA	ENSP00000424103.2:n.382+156_382+157insA
ENST00000673642.1:c.430+156_430+157insA	ENSP00000501242.1:n.430+156_430+157insA
ENST00000673991.1:c.631+156_631+157insA	ENSP00000501033.1:n.631+156_631+157insA
ENST00000226760.5:c.631+156_631+157insA MANE Select	ENSP00000226760.1:n.631+156_631+157insA
ENST00000503569.5:c.631+156_631+157insA	ENSP00000423337.1:n.631+156_631+157insA
ENST00000506362.1:c.228+156_228+157insA
ENST00000507765.1:n.816+156_816+157insA
NM_001145853.1:c.631+156_631+157insA	NP_001139325.1:n.631+156_631+157insA
NM_006005.3:c.631+156_631+157insA MANE Select	NP_005996.2:n.631+156_631+157insA
XM_017008586.1:c.640+156_640+157insA	XP_016864075.1:n.640+156_640+157insA