Canonical Allele Identifier: CA356175204

Gene: WFS1

Linked Data

• ClinVar Variation Id: 1341636
• ClinVar RCV Id: RCV001837132
• dbSNP Id: rs1343901456
• gnomAD v2: 4-6303023-G-A
• gnomAD v3: 4-6301296-G-A
• gnomAD v4: 4-6301296-G-A
• MyVariant Identifiers: chr4:g.6303023G>A (hg19) ; chr4:g.6301296G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301296G>A , CM000666.2:g.6301296G>A	GRCh38
NC_000004.11:g.6303023G>A , CM000666.1:g.6303023G>A	GRCh37
NC_000004.10:g.6353924G>A	NCBI36
NG_011700.1:g.36447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1537G>A	ENSP00000507852.1:p.Val513Ile
ENST00000683395.1:c.1478G>A
ENST00000684087.1:c.1501G>A	ENSP00000506978.1:p.Val501Ile
ENST00000506362.2:c.1252G>A	ENSP00000424103.2:p.Val418Ile
ENST00000673642.1:c.1160G>A	ENSP00000501242.1:p.Arg387His
ENST00000673991.1:c.1537G>A	ENSP00000501033.1:p.Val513Ile
ENST00000226760.5:c.1501G>A MANE Select	ENSP00000226760.1:p.Val501Ile
ENST00000503569.5:c.1501G>A	ENSP00000423337.1:p.Val501Ile
ENST00000507765.1:n.1686G>A
NM_001145853.1:c.1501G>A	NP_001139325.1:p.Val501Ile
NM_006005.3:c.1501G>A MANE Select	NP_005996.2:p.Val501Ile
XM_017008586.1:c.1510G>A	XP_016864075.1:p.Val504Ile