Canonical Allele Identifier: CA2669843956

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302923-A-AGCAGCTCTTCCCCTTTCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302925_6302943dup , CM000666.2:g.6302925_6302943dup	GRCh38
NC_000004.11:g.6304652_6304670dup , CM000666.1:g.6304652_6304670dup	GRCh37
NC_000004.10:g.6355553_6355571dup	NCBI36
NG_011700.1:g.38076_38094dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*457_*475dup	ENSP00000507852.1:n.*457_*475dup
ENST00000683395.1:c.3107_3125dup
ENST00000684087.1:c.*457_*475dup	ENSP00000506978.1:n.*457_*475dup
ENST00000673991.1:c.*457_*475dup	ENSP00000501033.1:n.*457_*475dup
ENST00000226760.5:c.*457_*475dup MANE Select	ENSP00000226760.1:n.*457_*475dup
ENST00000507765.1:n.3315_3333dup
NM_001145853.1:c.*457_*475dup	NP_001139325.1:n.*457_*475dup
NM_006005.3:c.*457_*475dup MANE Select	NP_005996.2:n.*457_*475dup
XM_017008586.1:c.*457_*475dup	XP_016864075.1:n.*457_*475dup
XR_001741566.2:n.2003_2021dup