Canonical Allele Identifier: CA356174430

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6302713C>A (hg19) ; chr4:g.6300986C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300986C>A , CM000666.2:g.6300986C>A	GRCh38
NC_000004.11:g.6302713C>A , CM000666.1:g.6302713C>A	GRCh37
NC_000004.10:g.6353614C>A	NCBI36
NG_011700.1:g.36137C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1227C>A	ENSP00000507852.1:p.Phe409Leu
ENST00000683395.1:c.1168C>A
ENST00000684087.1:c.1191C>A	ENSP00000506978.1:p.Phe397Leu
ENST00000506362.2:c.942C>A	ENSP00000424103.2:p.Phe314Leu
ENST00000673642.1:c.850C>A	ENSP00000501242.1:p.Arg284=
ENST00000673991.1:c.1227C>A	ENSP00000501033.1:p.Phe409Leu
ENST00000226760.5:c.1191C>A MANE Select	ENSP00000226760.1:p.Phe397Leu
ENST00000503569.5:c.1191C>A	ENSP00000423337.1:p.Phe397Leu
ENST00000507765.1:n.1376C>A
NM_001145853.1:c.1191C>A	NP_001139325.1:p.Phe397Leu
NM_006005.3:c.1191C>A MANE Select	NP_005996.2:p.Phe397Leu
XM_017008586.1:c.1200C>A	XP_016864075.1:p.Phe400Leu