Canonical Allele Identifier: CA2760285123
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301479_6301480insT , CM000666.2:g.6301479_6301480insT GRCh38
NC_000004.11:g.6303206_6303207insT , CM000666.1:g.6303206_6303207insT GRCh37
NC_000004.10:g.6354107_6354108insT NCBI36
NG_011700.1:g.36630_36631insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1720_1721insT ENSP00000507852.1:p.Gly574ValfsTer?
ENST00000683395.1:c.1661_1662insT
ENST00000684087.1:c.1684_1685insT ENSP00000506978.1:p.Gly562ValfsTer?
ENST00000506362.2:c.1435_1436insT ENSP00000424103.2:p.Gly479ValfsTer?
ENST00000673642.1:c.1343_1344insT ENSP00000501242.1:n.1343_1344insT
ENST00000673991.1:c.1720_1721insT ENSP00000501033.1:p.Gly574ValfsTer?
ENST00000226760.5:c.1684_1685insT MANE Select ENSP00000226760.1:p.Gly562ValfsTer?
ENST00000503569.5:c.1684_1685insT ENSP00000423337.1:p.Gly562ValfsTer?
ENST00000507765.1:n.1869_1870insT
NM_001145853.1:c.1684_1685insT NP_001139325.1:p.Gly562ValfsTer?
NM_006005.3:c.1684_1685insT MANE Select NP_005996.2:p.Gly562ValfsTer?
XM_017008586.1:c.1693_1694insT XP_016864075.1:p.Gly565ValfsTer?