Canonical Allele Identifier: CA2669843893

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302825-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302827_6302828del , CM000666.2:g.6302827_6302828del	GRCh38
NC_000004.11:g.6304554_6304555del , CM000666.1:g.6304554_6304555del	GRCh37
NC_000004.10:g.6355455_6355456del	NCBI36
NG_011700.1:g.37978_37979del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*359_*360del	ENSP00000507852.1:n.*359_*360del
ENST00000683395.1:c.3009_3010del
ENST00000684087.1:c.*359_*360del	ENSP00000506978.1:n.*359_*360del
ENST00000506362.2:c.*359_*360del	ENSP00000424103.2:n.*359_*360del
ENST00000673991.1:c.*359_*360del	ENSP00000501033.1:n.*359_*360del
ENST00000226760.5:c.*359_*360del MANE Select	ENSP00000226760.1:n.*359_*360del
ENST00000503569.5:c.*359_*360del	ENSP00000423337.1:n.*359_*360del
ENST00000507765.1:n.3217_3218del
NM_001145853.1:c.*359_*360del	NP_001139325.1:n.*359_*360del
NM_006005.3:c.*359_*360del MANE Select	NP_005996.2:n.*359_*360del
XM_017008586.1:c.*359_*360del	XP_016864075.1:n.*359_*360del