Canonical Allele Identifier: CA321956

Gene: WFS1

Linked Data

• dbSNP Id: rs1553879080
• COSMIC: COSM3604881
• MyVariant Identifiers: chr4:g.6304104T>G (hg19) ; chr4:g.6302377T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302377T>G , CM000666.2:g.6302377T>G	GRCh38
NC_000004.11:g.6304104T>G , CM000666.1:g.6304104T>G	GRCh37
NC_000004.10:g.6355005T>G	NCBI36
NG_011700.1:g.37528T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2618T>G	ENSP00000507852.1:p.Val873Gly
ENST00000683395.1:c.2559T>G
ENST00000684087.1:c.2582T>G	ENSP00000506978.1:p.Val861Gly
ENST00000506362.2:c.2333T>G	ENSP00000424103.2:p.Val778Gly
ENST00000673991.1:c.2618T>G	ENSP00000501033.1:p.Val873Gly
ENST00000226760.5:c.2582T>G MANE Select	ENSP00000226760.1:p.Val861Gly
ENST00000503569.5:c.2582T>G	ENSP00000423337.1:p.Val861Gly
ENST00000507765.1:n.2767T>G
NM_001145853.1:c.2582T>G	NP_001139325.1:p.Val861Gly
NM_006005.3:c.2582T>G MANE Select	NP_005996.2:p.Val861Gly
XM_017008586.1:c.2591T>G	XP_016864075.1:p.Val864Gly