Canonical Allele Identifier: CA136326

Gene: WFS1

Linked Data

• ClinVar Variation Id: 45429
• ClinVar RCV Id: RCV000038633 ; RCV001775561 ; RCV002509034
• dbSNP Id: rs397517194
• ExAC: 4:6302625 G / A
• gnomAD v2: 4-6302625-G-A
• gnomAD v3: 4-6300898-G-A
• gnomAD v4: 4-6300898-G-A
• MyVariant Identifiers: chr4:g.6302625G>A (hg19) ; chr4:g.6300898G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300898G>A , CM000666.2:g.6300898G>A	GRCh38
NC_000004.11:g.6302625G>A , CM000666.1:g.6302625G>A	GRCh37
NC_000004.10:g.6353526G>A	NCBI36
NG_011700.1:g.36049G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1139G>A	ENSP00000507852.1:p.Ser380Asn
ENST00000683395.1:c.1080G>A
ENST00000684087.1:c.1103G>A	ENSP00000506978.1:p.Ser368Asn
ENST00000506362.2:c.854G>A	ENSP00000424103.2:p.Ser285Asn
ENST00000673642.1:c.762G>A	ENSP00000501242.1:p.Gln254=
ENST00000673991.1:c.1139G>A	ENSP00000501033.1:p.Ser380Asn
ENST00000226760.5:c.1103G>A MANE Select	ENSP00000226760.1:p.Ser368Asn
ENST00000503569.5:c.1103G>A	ENSP00000423337.1:p.Ser368Asn
ENST00000506362.1:c.736G>A
ENST00000507765.1:n.1288G>A
NM_001145853.1:c.1103G>A	NP_001139325.1:p.Ser368Asn
NM_006005.3:c.1103G>A MANE Select	NP_005996.2:p.Ser368Asn
XM_017008586.1:c.1112G>A	XP_016864075.1:p.Ser371Asn