Canonical Allele Identifier: CA2669843953

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302920-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302922del , CM000666.2:g.6302922del	GRCh38
NC_000004.11:g.6304649del , CM000666.1:g.6304649del	GRCh37
NC_000004.10:g.6355550del	NCBI36
NG_011700.1:g.38073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*454del	ENSP00000507852.1:n.*454del
ENST00000683395.1:c.3104del
ENST00000684087.1:c.*454del	ENSP00000506978.1:n.*454del
ENST00000673991.1:c.*454del	ENSP00000501033.1:n.*454del
ENST00000226760.5:c.*454del MANE Select	ENSP00000226760.1:n.*454del
ENST00000507765.1:n.3312del
NM_001145853.1:c.*454del	NP_001139325.1:n.*454del
NM_006005.3:c.*454del MANE Select	NP_005996.2:n.*454del
XM_017008586.1:c.*454del	XP_016864075.1:n.*454del
XR_001741566.2:n.2024del