Canonical Allele Identifier: CA356174380

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6302688A>T (hg19) ; chr4:g.6300961A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300961A>T , CM000666.2:g.6300961A>T	GRCh38
NC_000004.11:g.6302688A>T , CM000666.1:g.6302688A>T	GRCh37
NC_000004.10:g.6353589A>T	NCBI36
NG_011700.1:g.36112A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1202A>T	ENSP00000507852.1:p.Asp401Val
ENST00000683395.1:c.1143A>T
ENST00000684087.1:c.1166A>T	ENSP00000506978.1:p.Asp389Val
ENST00000506362.2:c.917A>T	ENSP00000424103.2:p.Asp306Val
ENST00000673642.1:c.825A>T	ENSP00000501242.1:p.Gly275=
ENST00000673991.1:c.1202A>T	ENSP00000501033.1:p.Asp401Val
ENST00000226760.5:c.1166A>T MANE Select	ENSP00000226760.1:p.Asp389Val
ENST00000503569.5:c.1166A>T	ENSP00000423337.1:p.Asp389Val
ENST00000507765.1:n.1351A>T
NM_001145853.1:c.1166A>T	NP_001139325.1:p.Asp389Val
NM_006005.3:c.1166A>T MANE Select	NP_005996.2:p.Asp389Val
XM_017008586.1:c.1175A>T	XP_016864075.1:p.Asp392Val