Canonical Allele Identifier: CA1435773193

Gene: WFS1

Linked Data

• dbSNP Id: rs1731008774
• gnomAD v3: 4-6302779-AGAT-A
• gnomAD v4: 4-6302779-AGAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302782_6302784del , CM000666.2:g.6302782_6302784del	GRCh38
NC_000004.11:g.6304509_6304511del , CM000666.1:g.6304509_6304511del	GRCh37
NC_000004.10:g.6355410_6355412del	NCBI36
NG_011700.1:g.37933_37935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*314_*316del	ENSP00000507852.1:n.*314_*316del
ENST00000683395.1:c.2964_2966del
ENST00000684087.1:c.*314_*316del	ENSP00000506978.1:n.*314_*316del
ENST00000506362.2:c.*314_*316del	ENSP00000424103.2:n.*314_*316del
ENST00000673991.1:c.*314_*316del	ENSP00000501033.1:n.*314_*316del
ENST00000226760.5:c.*314_*316del MANE Select	ENSP00000226760.1:n.*314_*316del
ENST00000503569.5:c.*314_*316del	ENSP00000423337.1:n.*314_*316del
ENST00000507765.1:n.3172_3174del
NM_001145853.1:c.*314_*316del	NP_001139325.1:n.*314_*316del
NM_006005.3:c.*314_*316del MANE Select	NP_005996.2:n.*314_*316del
XM_017008586.1:c.*314_*316del	XP_016864075.1:n.*314_*316del