Canonical Allele Identifier: CA91796630

Gene: WFS1

Linked Data

• ClinVar Variation Id: 631948
• ClinVar RCV Id: RCV000778740 ; RCV003546599
• dbSNP Id: rs775158434
• gnomAD v2: 4-6303358-G-A
• gnomAD v3: 4-6301631-G-A
• gnomAD v4: 4-6301631-G-A
• MyVariant Identifiers: chr4:g.6303358G>A (hg19) ; chr4:g.6301631G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301631G>A , CM000666.2:g.6301631G>A	GRCh38
NC_000004.11:g.6303358G>A , CM000666.1:g.6303358G>A	GRCh37
NC_000004.10:g.6354259G>A	NCBI36
NG_011700.1:g.36782G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1872G>A	ENSP00000507852.1:p.Trp624Ter
ENST00000683395.1:c.1813G>A
ENST00000684087.1:c.1836G>A	ENSP00000506978.1:p.Trp612Ter
ENST00000506362.2:c.1587G>A	ENSP00000424103.2:p.Trp529Ter
ENST00000673642.1:c.1495G>A	ENSP00000501242.1:n.1495G>A
ENST00000673991.1:c.1872G>A	ENSP00000501033.1:p.Trp624Ter
ENST00000226760.5:c.1836G>A MANE Select	ENSP00000226760.1:p.Trp612Ter
ENST00000503569.5:c.1836G>A	ENSP00000423337.1:p.Trp612Ter
ENST00000507765.1:n.2021G>A
NM_001145853.1:c.1836G>A	NP_001139325.1:p.Trp612Ter
NM_006005.3:c.1836G>A MANE Select	NP_005996.2:p.Trp612Ter
XM_017008586.1:c.1845G>A	XP_016864075.1:p.Trp615Ter