Canonical Allele Identifier: CA2669843592

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302582-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302584dup , CM000666.2:g.6302584dup	GRCh38
NC_000004.11:g.6304311dup , CM000666.1:g.6304311dup	GRCh37
NC_000004.10:g.6355212dup	NCBI36
NG_011700.1:g.37735dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*116dup	ENSP00000507852.1:n.*116dup
ENST00000683395.1:c.2766dup
ENST00000684087.1:c.*116dup	ENSP00000506978.1:n.*116dup
ENST00000506362.2:c.*116dup	ENSP00000424103.2:n.*116dup
ENST00000673991.1:c.*116dup	ENSP00000501033.1:n.*116dup
ENST00000226760.5:c.*116dup MANE Select	ENSP00000226760.1:n.*116dup
ENST00000503569.5:c.*116dup	ENSP00000423337.1:n.*116dup
ENST00000507765.1:n.2974dup
NM_001145853.1:c.*116dup	NP_001139325.1:n.*116dup
NM_006005.3:c.*116dup MANE Select	NP_005996.2:n.*116dup
XM_017008586.1:c.*116dup	XP_016864075.1:n.*116dup