Canonical Allele Identifier: CA2760283896

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291452_6291453insA , CM000666.2:g.6291452_6291453insA	GRCh38
NC_000004.11:g.6293179_6293180insA , CM000666.1:g.6293179_6293180insA	GRCh37
NC_000004.10:g.6344080_6344081insA	NCBI36
NG_011700.1:g.26603_26604insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+85_631+86insA	ENSP00000507852.1:n.631+85_631+86insA
ENST00000683395.1:c.608+98_608+99insA
ENST00000684087.1:c.631+85_631+86insA	ENSP00000506978.1:n.631+85_631+86insA
ENST00000684700.1:c.*11_*12insA	ENSP00000507806.1:n.*11_*12insA
ENST00000506362.2:c.382+85_382+86insA	ENSP00000424103.2:n.382+85_382+86insA
ENST00000673642.1:c.430+85_430+86insA	ENSP00000501242.1:n.430+85_430+86insA
ENST00000673991.1:c.631+85_631+86insA	ENSP00000501033.1:n.631+85_631+86insA
ENST00000226760.5:c.631+85_631+86insA MANE Select	ENSP00000226760.1:n.631+85_631+86insA
ENST00000503569.5:c.631+85_631+86insA	ENSP00000423337.1:n.631+85_631+86insA
ENST00000506362.1:c.228+85_228+86insA
ENST00000507765.1:n.816+85_816+86insA
NM_001145853.1:c.631+85_631+86insA	NP_001139325.1:n.631+85_631+86insA
NM_006005.3:c.631+85_631+86insA MANE Select	NP_005996.2:n.631+85_631+86insA
XM_017008586.1:c.640+85_640+86insA	XP_016864075.1:n.640+85_640+86insA