Canonical Allele Identifier: CA325363

Gene: WFS1

Linked Data

• ClinVar Variation Id: 215411
• ClinVar RCV Id: RCV000200779
• dbSNP Id: rs863224269
• MyVariant Identifiers: chr4:g.6302714G>C (hg19) ; chr4:g.6300987G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300987G>C , CM000666.2:g.6300987G>C	GRCh38
NC_000004.11:g.6302714G>C , CM000666.1:g.6302714G>C	GRCh37
NC_000004.10:g.6353615G>C	NCBI36
NG_011700.1:g.36138G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1228G>C	ENSP00000507852.1:p.Gly410Arg
ENST00000683395.1:c.1169G>C
ENST00000684087.1:c.1192G>C	ENSP00000506978.1:p.Gly398Arg
ENST00000506362.2:c.943G>C	ENSP00000424103.2:p.Gly315Arg
ENST00000673642.1:c.851G>C	ENSP00000501242.1:p.Arg284Pro
ENST00000673991.1:c.1228G>C	ENSP00000501033.1:p.Gly410Arg
ENST00000226760.5:c.1192G>C MANE Select	ENSP00000226760.1:p.Gly398Arg
ENST00000503569.5:c.1192G>C	ENSP00000423337.1:p.Gly398Arg
ENST00000507765.1:n.1377G>C
NM_001145853.1:c.1192G>C	NP_001139325.1:p.Gly398Arg
NM_006005.3:c.1192G>C MANE Select	NP_005996.2:p.Gly398Arg
XM_017008586.1:c.1201G>C	XP_016864075.1:p.Gly401Arg