Canonical Allele Identifier: CA2760284104

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291568_6291569insA , CM000666.2:g.6291568_6291569insA	GRCh38
NC_000004.11:g.6293295_6293296insA , CM000666.1:g.6293295_6293296insA	GRCh37
NC_000004.10:g.6344196_6344197insA	NCBI36
NG_011700.1:g.26719_26720insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+201_631+202insA	ENSP00000507852.1:n.631+201_631+202insA
ENST00000683395.1:c.608+214_608+215insA
ENST00000684087.1:c.631+201_631+202insA	ENSP00000506978.1:n.631+201_631+202insA
ENST00000684700.1:c.*127_*128insA	ENSP00000507806.1:n.*127_*128insA
ENST00000506362.2:c.382+201_382+202insA	ENSP00000424103.2:n.382+201_382+202insA
ENST00000673642.1:c.430+201_430+202insA	ENSP00000501242.1:n.430+201_430+202insA
ENST00000673991.1:c.631+201_631+202insA	ENSP00000501033.1:n.631+201_631+202insA
ENST00000226760.5:c.631+201_631+202insA MANE Select	ENSP00000226760.1:n.631+201_631+202insA
ENST00000503569.5:c.631+201_631+202insA	ENSP00000423337.1:n.631+201_631+202insA
ENST00000506362.1:c.228+201_228+202insA
ENST00000507765.1:n.816+201_816+202insA
NM_001145853.1:c.631+201_631+202insA	NP_001139325.1:n.631+201_631+202insA
NM_006005.3:c.631+201_631+202insA MANE Select	NP_005996.2:n.631+201_631+202insA
XM_017008586.1:c.640+201_640+202insA	XP_016864075.1:n.640+201_640+202insA