Canonical Allele Identifier: CA2760283911

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291465_6291476del , CM000666.2:g.6291465_6291476del	GRCh38
NC_000004.11:g.6293192_6293203del , CM000666.1:g.6293192_6293203del	GRCh37
NC_000004.10:g.6344093_6344104del	NCBI36
NG_011700.1:g.26616_26627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+98_631+109del	ENSP00000507852.1:n.631+98_631+109del
ENST00000683395.1:c.608+111_608+122del
ENST00000684087.1:c.631+98_631+109del	ENSP00000506978.1:n.631+98_631+109del
ENST00000684700.1:c.*24_*35del	ENSP00000507806.1:n.*24_*35del
ENST00000506362.2:c.382+98_382+109del	ENSP00000424103.2:n.382+98_382+109del
ENST00000673642.1:c.430+98_430+109del	ENSP00000501242.1:n.430+98_430+109del
ENST00000673991.1:c.631+98_631+109del	ENSP00000501033.1:n.631+98_631+109del
ENST00000226760.5:c.631+98_631+109del MANE Select	ENSP00000226760.1:n.631+98_631+109del
ENST00000503569.5:c.631+98_631+109del	ENSP00000423337.1:n.631+98_631+109del
ENST00000506362.1:c.228+98_228+109del
ENST00000507765.1:n.816+98_816+109del
NM_001145853.1:c.631+98_631+109del	NP_001139325.1:n.631+98_631+109del
NM_006005.3:c.631+98_631+109del MANE Select	NP_005996.2:n.631+98_631+109del
XM_017008586.1:c.640+98_640+109del	XP_016864075.1:n.640+98_640+109del