Canonical Allele Identifier: CA2760284107

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291571_6291572insACA , CM000666.2:g.6291571_6291572insACA	GRCh38
NC_000004.11:g.6293298_6293299insACA , CM000666.1:g.6293298_6293299insACA	GRCh37
NC_000004.10:g.6344199_6344200insACA	NCBI36
NG_011700.1:g.26722_26723insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+204_631+205insACA	ENSP00000507852.1:n.631+204_631+205insACA
ENST00000683395.1:c.608+217_608+218insACA
ENST00000684087.1:c.631+204_631+205insACA	ENSP00000506978.1:n.631+204_631+205insACA
ENST00000684700.1:c.*130_*131insACA	ENSP00000507806.1:n.*130_*131insACA
ENST00000506362.2:c.382+204_382+205insACA	ENSP00000424103.2:n.382+204_382+205insACA
ENST00000673642.1:c.430+204_430+205insACA	ENSP00000501242.1:n.430+204_430+205insACA
ENST00000673991.1:c.631+204_631+205insACA	ENSP00000501033.1:n.631+204_631+205insACA
ENST00000226760.5:c.631+204_631+205insACA MANE Select	ENSP00000226760.1:n.631+204_631+205insACA
ENST00000503569.5:c.631+204_631+205insACA	ENSP00000423337.1:n.631+204_631+205insACA
ENST00000506362.1:c.228+204_228+205insACA
ENST00000507765.1:n.816+204_816+205insACA
NM_001145853.1:c.631+204_631+205insACA	NP_001139325.1:n.631+204_631+205insACA
NM_006005.3:c.631+204_631+205insACA MANE Select	NP_005996.2:n.631+204_631+205insACA
XM_017008586.1:c.640+204_640+205insACA	XP_016864075.1:n.640+204_640+205insACA