Canonical Allele Identifier: CA2760284131

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291602_6291607del , CM000666.2:g.6291602_6291607del	GRCh38
NC_000004.11:g.6293329_6293334del , CM000666.1:g.6293329_6293334del	GRCh37
NC_000004.10:g.6344230_6344235del	NCBI36
NG_011700.1:g.26753_26758del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+235_631+240del	ENSP00000507852.1:n.631+235_631+240del
ENST00000683395.1:c.608+248_608+253del
ENST00000684087.1:c.631+235_631+240del	ENSP00000506978.1:n.631+235_631+240del
ENST00000684700.1:c.*161_*166del	ENSP00000507806.1:n.*161_*166del
ENST00000506362.2:c.382+235_382+240del	ENSP00000424103.2:n.382+235_382+240del
ENST00000673642.1:c.430+235_430+240del	ENSP00000501242.1:n.430+235_430+240del
ENST00000673991.1:c.631+235_631+240del	ENSP00000501033.1:n.631+235_631+240del
ENST00000226760.5:c.631+235_631+240del MANE Select	ENSP00000226760.1:n.631+235_631+240del
ENST00000503569.5:c.631+235_631+240del	ENSP00000423337.1:n.631+235_631+240del
ENST00000506362.1:c.228+235_228+240del
ENST00000507765.1:n.816+235_816+240del
NM_001145853.1:c.631+235_631+240del	NP_001139325.1:n.631+235_631+240del
NM_006005.3:c.631+235_631+240del MANE Select	NP_005996.2:n.631+235_631+240del
XM_017008586.1:c.640+235_640+240del	XP_016864075.1:n.640+235_640+240del