Canonical Allele Identifier: CA2760284084

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291556_6291557insACT , CM000666.2:g.6291556_6291557insACT	GRCh38
NC_000004.11:g.6293283_6293284insACT , CM000666.1:g.6293283_6293284insACT	GRCh37
NC_000004.10:g.6344184_6344185insACT	NCBI36
NG_011700.1:g.26707_26708insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+189_631+190insACT	ENSP00000507852.1:n.631+189_631+190insACT
ENST00000683395.1:c.608+202_608+203insACT
ENST00000684087.1:c.631+189_631+190insACT	ENSP00000506978.1:n.631+189_631+190insACT
ENST00000684700.1:c.*115_*116insACT	ENSP00000507806.1:n.*115_*116insACT
ENST00000506362.2:c.382+189_382+190insACT	ENSP00000424103.2:n.382+189_382+190insACT
ENST00000673642.1:c.430+189_430+190insACT	ENSP00000501242.1:n.430+189_430+190insACT
ENST00000673991.1:c.631+189_631+190insACT	ENSP00000501033.1:n.631+189_631+190insACT
ENST00000226760.5:c.631+189_631+190insACT MANE Select	ENSP00000226760.1:n.631+189_631+190insACT
ENST00000503569.5:c.631+189_631+190insACT	ENSP00000423337.1:n.631+189_631+190insACT
ENST00000506362.1:c.228+189_228+190insACT
ENST00000507765.1:n.816+189_816+190insACT
NM_001145853.1:c.631+189_631+190insACT	NP_001139325.1:n.631+189_631+190insACT
NM_006005.3:c.631+189_631+190insACT MANE Select	NP_005996.2:n.631+189_631+190insACT
XM_017008586.1:c.640+189_640+190insACT	XP_016864075.1:n.640+189_640+190insACT