Canonical Allele Identifier: CA2760284068

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291551_6291556del , CM000666.2:g.6291551_6291556del	GRCh38
NC_000004.11:g.6293278_6293283del , CM000666.1:g.6293278_6293283del	GRCh37
NC_000004.10:g.6344179_6344184del	NCBI36
NG_011700.1:g.26702_26707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+184_631+189del	ENSP00000507852.1:n.631+184_631+189del
ENST00000683395.1:c.608+197_608+202del
ENST00000684087.1:c.631+184_631+189del	ENSP00000506978.1:n.631+184_631+189del
ENST00000684700.1:c.*110_*115del	ENSP00000507806.1:n.*110_*115del
ENST00000506362.2:c.382+184_382+189del	ENSP00000424103.2:n.382+184_382+189del
ENST00000673642.1:c.430+184_430+189del	ENSP00000501242.1:n.430+184_430+189del
ENST00000673991.1:c.631+184_631+189del	ENSP00000501033.1:n.631+184_631+189del
ENST00000226760.5:c.631+184_631+189del MANE Select	ENSP00000226760.1:n.631+184_631+189del
ENST00000503569.5:c.631+184_631+189del	ENSP00000423337.1:n.631+184_631+189del
ENST00000506362.1:c.228+184_228+189del
ENST00000507765.1:n.816+184_816+189del
NM_001145853.1:c.631+184_631+189del	NP_001139325.1:n.631+184_631+189del
NM_006005.3:c.631+184_631+189del MANE Select	NP_005996.2:n.631+184_631+189del
XM_017008586.1:c.640+184_640+189del	XP_016864075.1:n.640+184_640+189del