Canonical Allele Identifier: CA356175234

Gene: WFS1

Linked Data

• dbSNP Id: rs573775230
• gnomAD v2: 4-6303029-G-T
• gnomAD v4: 4-6301302-G-T
• MyVariant Identifiers: chr4:g.6303029G>T (hg19) ; chr4:g.6301302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301302G>T , CM000666.2:g.6301302G>T	GRCh38
NC_000004.11:g.6303029G>T , CM000666.1:g.6303029G>T	GRCh37
NC_000004.10:g.6353930G>T	NCBI36
NG_011700.1:g.36453G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1543G>T	ENSP00000507852.1:p.Val515Phe
ENST00000683395.1:c.1484G>T
ENST00000684087.1:c.1507G>T	ENSP00000506978.1:p.Val503Phe
ENST00000506362.2:c.1258G>T	ENSP00000424103.2:p.Val420Phe
ENST00000673642.1:c.1166G>T	ENSP00000501242.1:p.Arg389Leu
ENST00000673991.1:c.1543G>T	ENSP00000501033.1:p.Val515Phe
ENST00000226760.5:c.1507G>T MANE Select	ENSP00000226760.1:p.Val503Phe
ENST00000503569.5:c.1507G>T	ENSP00000423337.1:p.Val503Phe
ENST00000507765.1:n.1692G>T
NM_001145853.1:c.1507G>T	NP_001139325.1:p.Val503Phe
NM_006005.3:c.1507G>T MANE Select	NP_005996.2:p.Val503Phe
XM_017008586.1:c.1516G>T	XP_016864075.1:p.Val506Phe