Canonical Allele Identifier: CA356175131

Gene: WFS1

Linked Data

• ClinVar Variation Id: 2181636
• ClinVar RCV Id: RCV002606248
• MyVariant Identifiers: chr4:g.6303002G>T (hg19) ; chr4:g.6301275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301275G>T , CM000666.2:g.6301275G>T	GRCh38
NC_000004.11:g.6303002G>T , CM000666.1:g.6303002G>T	GRCh37
NC_000004.10:g.6353903G>T	NCBI36
NG_011700.1:g.36426G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1516G>T	ENSP00000507852.1:p.Gly506Cys
ENST00000683395.1:c.1457G>T
ENST00000684087.1:c.1480G>T	ENSP00000506978.1:p.Gly494Cys
ENST00000506362.2:c.1231G>T	ENSP00000424103.2:p.Gly411Cys
ENST00000673642.1:c.1139G>T	ENSP00000501242.1:p.Arg380Leu
ENST00000673991.1:c.1516G>T	ENSP00000501033.1:p.Gly506Cys
ENST00000226760.5:c.1480G>T MANE Select	ENSP00000226760.1:p.Gly494Cys
ENST00000503569.5:c.1480G>T	ENSP00000423337.1:p.Gly494Cys
ENST00000507765.1:n.1665G>T
NM_001145853.1:c.1480G>T	NP_001139325.1:p.Gly494Cys
NM_006005.3:c.1480G>T MANE Select	NP_005996.2:p.Gly494Cys
XM_017008586.1:c.1489G>T	XP_016864075.1:p.Gly497Cys