Canonical Allele Identifier: CA356178169

Gene: WFS1

Linked Data

• dbSNP Id: rs71532865
• gnomAD v2: 4-6303746-T-G
• gnomAD v4: 4-6302019-T-G
• MyVariant Identifiers: chr4:g.6303746T>G (hg19) ; chr4:g.6302019T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302019T>G , CM000666.2:g.6302019T>G	GRCh38
NC_000004.11:g.6303746T>G , CM000666.1:g.6303746T>G	GRCh37
NC_000004.10:g.6354647T>G	NCBI36
NG_011700.1:g.37170T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2260T>G	ENSP00000507852.1:p.Cys754Gly
ENST00000683395.1:c.2201T>G
ENST00000684087.1:c.2224T>G	ENSP00000506978.1:p.Cys742Gly
ENST00000506362.2:c.1975T>G	ENSP00000424103.2:p.Cys659Gly
ENST00000673642.1:c.1883T>G	ENSP00000501242.1:n.1883T>G
ENST00000673991.1:c.2260T>G	ENSP00000501033.1:p.Cys754Gly
ENST00000226760.5:c.2224T>G MANE Select	ENSP00000226760.1:p.Cys742Gly
ENST00000503569.5:c.2224T>G	ENSP00000423337.1:p.Cys742Gly
ENST00000507765.1:n.2409T>G
NM_001145853.1:c.2224T>G	NP_001139325.1:p.Cys742Gly
NM_006005.3:c.2224T>G MANE Select	NP_005996.2:p.Cys742Gly
XM_017008586.1:c.2233T>G	XP_016864075.1:p.Cys745Gly