Canonical Allele Identifier: CA2760283909

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291464_6291465insACT , CM000666.2:g.6291464_6291465insACT	GRCh38
NC_000004.11:g.6293191_6293192insACT , CM000666.1:g.6293191_6293192insACT	GRCh37
NC_000004.10:g.6344092_6344093insACT	NCBI36
NG_011700.1:g.26615_26616insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+97_631+98insACT	ENSP00000507852.1:n.631+97_631+98insACT
ENST00000683395.1:c.608+110_608+111insACT
ENST00000684087.1:c.631+97_631+98insACT	ENSP00000506978.1:n.631+97_631+98insACT
ENST00000684700.1:c.*23_*24insACT	ENSP00000507806.1:n.*23_*24insACT
ENST00000506362.2:c.382+97_382+98insACT	ENSP00000424103.2:n.382+97_382+98insACT
ENST00000673642.1:c.430+97_430+98insACT	ENSP00000501242.1:n.430+97_430+98insACT
ENST00000673991.1:c.631+97_631+98insACT	ENSP00000501033.1:n.631+97_631+98insACT
ENST00000226760.5:c.631+97_631+98insACT MANE Select	ENSP00000226760.1:n.631+97_631+98insACT
ENST00000503569.5:c.631+97_631+98insACT	ENSP00000423337.1:n.631+97_631+98insACT
ENST00000506362.1:c.228+97_228+98insACT
ENST00000507765.1:n.816+97_816+98insACT
NM_001145853.1:c.631+97_631+98insACT	NP_001139325.1:n.631+97_631+98insACT
NM_006005.3:c.631+97_631+98insACT MANE Select	NP_005996.2:n.631+97_631+98insACT
XM_017008586.1:c.640+97_640+98insACT	XP_016864075.1:n.640+97_640+98insACT