Canonical Allele Identifier: CA356176267

Gene: WFS1

Linked Data

• ClinVar Variation Id: 591231
• ClinVar RCV Id: RCV000722408 ; RCV003126921
• dbSNP Id: rs1560419651
• MyVariant Identifiers: chr4:g.6303135T>C (hg19) ; chr4:g.6301408T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301408T>C , CM000666.2:g.6301408T>C	GRCh38
NC_000004.11:g.6303135T>C , CM000666.1:g.6303135T>C	GRCh37
NC_000004.10:g.6354036T>C	NCBI36
NG_011700.1:g.36559T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1649T>C	ENSP00000507852.1:p.Phe550Ser
ENST00000683395.1:c.1590T>C
ENST00000684087.1:c.1613T>C	ENSP00000506978.1:p.Phe538Ser
ENST00000506362.2:c.1364T>C	ENSP00000424103.2:p.Phe455Ser
ENST00000673642.1:c.1272T>C	ENSP00000501242.1:p.Leu424=
ENST00000673991.1:c.1649T>C	ENSP00000501033.1:p.Phe550Ser
ENST00000226760.5:c.1613T>C MANE Select	ENSP00000226760.1:p.Phe538Ser
ENST00000503569.5:c.1613T>C	ENSP00000423337.1:p.Phe538Ser
ENST00000507765.1:n.1798T>C
NM_001145853.1:c.1613T>C	NP_001139325.1:p.Phe538Ser
NM_006005.3:c.1613T>C MANE Select	NP_005996.2:p.Phe538Ser
XM_017008586.1:c.1622T>C	XP_016864075.1:p.Phe541Ser