Canonical Allele Identifier: CA2760283993

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291511_6291517del , CM000666.2:g.6291511_6291517del	GRCh38
NC_000004.11:g.6293238_6293244del , CM000666.1:g.6293238_6293244del	GRCh37
NC_000004.10:g.6344139_6344145del	NCBI36
NG_011700.1:g.26662_26668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+144_631+150del	ENSP00000507852.1:n.631+144_631+150del
ENST00000683395.1:c.608+157_608+163del
ENST00000684087.1:c.631+144_631+150del	ENSP00000506978.1:n.631+144_631+150del
ENST00000684700.1:c.*70_*76del	ENSP00000507806.1:n.*70_*76del
ENST00000506362.2:c.382+144_382+150del	ENSP00000424103.2:n.382+144_382+150del
ENST00000673642.1:c.430+144_430+150del	ENSP00000501242.1:n.430+144_430+150del
ENST00000673991.1:c.631+144_631+150del	ENSP00000501033.1:n.631+144_631+150del
ENST00000226760.5:c.631+144_631+150del MANE Select	ENSP00000226760.1:n.631+144_631+150del
ENST00000503569.5:c.631+144_631+150del	ENSP00000423337.1:n.631+144_631+150del
ENST00000506362.1:c.228+144_228+150del
ENST00000507765.1:n.816+144_816+150del
NM_001145853.1:c.631+144_631+150del	NP_001139325.1:n.631+144_631+150del
NM_006005.3:c.631+144_631+150del MANE Select	NP_005996.2:n.631+144_631+150del
XM_017008586.1:c.640+144_640+150del	XP_016864075.1:n.640+144_640+150del