Canonical Allele Identifier: CA2586973609
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300966del , CM000666.2:g.6300966del GRCh38
NC_000004.11:g.6302693del , CM000666.1:g.6302693del GRCh37
NC_000004.10:g.6353594del NCBI36
NG_011700.1:g.36117del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1207del ENSP00000507852.1:p.Glu403SerfsTer?
ENST00000683395.1:c.1148del
ENST00000684087.1:c.1171del ENSP00000506978.1:p.Glu391SerfsTer?
ENST00000506362.2:c.922del ENSP00000424103.2:p.Glu308SerfsTer?
ENST00000673642.1:c.830del ENSP00000501242.1:p.Gly277GlufsTer?
ENST00000673991.1:c.1207del ENSP00000501033.1:p.Glu403SerfsTer?
ENST00000226760.5:c.1171del MANE Select ENSP00000226760.1:p.Glu391SerfsTer?
ENST00000503569.5:c.1171del ENSP00000423337.1:p.Glu391SerfsTer?
ENST00000507765.1:n.1356del
NM_001145853.1:c.1171del NP_001139325.1:p.Glu391SerfsTer?
NM_006005.3:c.1171del MANE Select NP_005996.2:p.Glu391SerfsTer?
XM_017008586.1:c.1180del XP_016864075.1:p.Glu394SerfsTer?