Canonical Allele Identifier: CA2841725580
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302296del , CM000666.2:g.6302296del GRCh38
NC_000004.11:g.6304023del , CM000666.1:g.6304023del GRCh37
NC_000004.10:g.6354924del NCBI36
NG_011700.1:g.37447del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2537del ENSP00000507852.1:p.Gly846AlafsTer28
ENST00000683395.1:c.2478del
ENST00000684087.1:c.2501del ENSP00000506978.1:p.Gly834AlafsTer28
ENST00000506362.2:c.2252del ENSP00000424103.2:p.Gly751AlafsTer28
ENST00000673991.1:c.2537del ENSP00000501033.1:p.Gly846AlafsTer28
ENST00000226760.5:c.2501del MANE Select ENSP00000226760.1:p.Gly834AlafsTer28
ENST00000503569.5:c.2501del ENSP00000423337.1:p.Gly834AlafsTer28
ENST00000507765.1:n.2686del
NM_001145853.1:c.2501del NP_001139325.1:p.Gly834AlafsTer28
NM_006005.3:c.2501del MANE Select NP_005996.2:p.Gly834AlafsTer28
XM_017008586.1:c.2510del XP_016864075.1:p.Gly837AlafsTer28