Canonical Allele Identifier: CA2669843485

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302484-A-AGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302485_6302488dup , CM000666.2:g.6302485_6302488dup	GRCh38
NC_000004.11:g.6304212_6304215dup , CM000666.1:g.6304212_6304215dup	GRCh37
NC_000004.10:g.6355113_6355116dup	NCBI36
NG_011700.1:g.37636_37639dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*17_*20dup	ENSP00000507852.1:n.*17_*20dup
ENST00000683395.1:c.2667_2670dup
ENST00000684087.1:c.*17_*20dup	ENSP00000506978.1:n.*17_*20dup
ENST00000506362.2:c.*17_*20dup	ENSP00000424103.2:n.*17_*20dup
ENST00000673991.1:c.*17_*20dup	ENSP00000501033.1:n.*17_*20dup
ENST00000226760.5:c.*17_*20dup MANE Select	ENSP00000226760.1:n.*17_*20dup
ENST00000503569.5:c.*17_*20dup	ENSP00000423337.1:n.*17_*20dup
ENST00000507765.1:n.2875_2878dup
NM_001145853.1:c.*17_*20dup	NP_001139325.1:n.*17_*20dup
NM_006005.3:c.*17_*20dup MANE Select	NP_005996.2:n.*17_*20dup
XM_017008586.1:c.*17_*20dup	XP_016864075.1:n.*17_*20dup