Canonical Allele Identifier: CA356174387

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6302691T>G (hg19) ; chr4:g.6300964T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300964T>G , CM000666.2:g.6300964T>G	GRCh38
NC_000004.11:g.6302691T>G , CM000666.1:g.6302691T>G	GRCh37
NC_000004.10:g.6353592T>G	NCBI36
NG_011700.1:g.36115T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1205T>G	ENSP00000507852.1:p.Val402Gly
ENST00000683395.1:c.1146T>G
ENST00000684087.1:c.1169T>G	ENSP00000506978.1:p.Val390Gly
ENST00000506362.2:c.920T>G	ENSP00000424103.2:p.Val307Gly
ENST00000673642.1:c.828T>G	ENSP00000501242.1:p.Cys276Trp
ENST00000673991.1:c.1205T>G	ENSP00000501033.1:p.Val402Gly
ENST00000226760.5:c.1169T>G MANE Select	ENSP00000226760.1:p.Val390Gly
ENST00000503569.5:c.1169T>G	ENSP00000423337.1:p.Val390Gly
ENST00000507765.1:n.1354T>G
NM_001145853.1:c.1169T>G	NP_001139325.1:p.Val390Gly
NM_006005.3:c.1169T>G MANE Select	NP_005996.2:p.Val390Gly
XM_017008586.1:c.1178T>G	XP_016864075.1:p.Val393Gly