Canonical Allele Identifier: CA645523670
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301707del , CM000666.2:g.6301707del GRCh38
NC_000004.11:g.6303434del , CM000666.1:g.6303434del GRCh37
NC_000004.10:g.6354335del NCBI36
NG_011700.1:g.36858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1948del ENSP00000507852.1:p.Val650CysfsTer20
ENST00000683395.1:c.1889del
ENST00000684087.1:c.1912del ENSP00000506978.1:p.Val638CysfsTer20
ENST00000506362.2:c.1663del ENSP00000424103.2:p.Val555CysfsTer20
ENST00000673642.1:c.1571del ENSP00000501242.1:n.1571del
ENST00000673991.1:c.1948del ENSP00000501033.1:p.Val650CysfsTer20
ENST00000226760.5:c.1912del MANE Select ENSP00000226760.1:p.Val638CysfsTer20
ENST00000503569.5:c.1912del ENSP00000423337.1:p.Val638CysfsTer20
ENST00000507765.1:n.2097del
NM_001145853.1:c.1912del NP_001139325.1:p.Val638CysfsTer20
NM_006005.3:c.1912del MANE Select NP_005996.2:p.Val638CysfsTer20
XM_017008586.1:c.1921del XP_016864075.1:p.Val641CysfsTer20