Canonical Allele Identifier: CA356177651

Gene: WFS1

Linked Data

• ClinVar Variation Id: 429213
• ClinVar RCV Id: RCV003126755
• dbSNP Id: rs1131691259
• gnomAD v2: 4-6303596-C-T
• gnomAD v3: 4-6301869-C-T
• gnomAD v4: 4-6301869-C-T
• MyVariant Identifiers: chr4:g.6303596C>T (hg19) ; chr4:g.6301869C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301869C>T , CM000666.2:g.6301869C>T	GRCh38
NC_000004.11:g.6303596C>T , CM000666.1:g.6303596C>T	GRCh37
NC_000004.10:g.6354497C>T	NCBI36
NG_011700.1:g.37020C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2110C>T	ENSP00000507852.1:p.His704Tyr
ENST00000683395.1:c.2051C>T
ENST00000684087.1:c.2074C>T	ENSP00000506978.1:p.His692Tyr
ENST00000506362.2:c.1825C>T	ENSP00000424103.2:p.His609Tyr
ENST00000673642.1:c.1733C>T	ENSP00000501242.1:n.1733C>T
ENST00000673991.1:c.2110C>T	ENSP00000501033.1:p.His704Tyr
ENST00000226760.5:c.2074C>T MANE Select	ENSP00000226760.1:p.His692Tyr
ENST00000503569.5:c.2074C>T	ENSP00000423337.1:p.His692Tyr
ENST00000507765.1:n.2259C>T
NM_001145853.1:c.2074C>T	NP_001139325.1:p.His692Tyr
NM_006005.3:c.2074C>T MANE Select	NP_005996.2:p.His692Tyr
XM_017008586.1:c.2083C>T	XP_016864075.1:p.His695Tyr