Canonical Allele Identifier: CA2586973655
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302281_6302291del , CM000666.2:g.6302281_6302291del GRCh38
NC_000004.11:g.6304008_6304018del , CM000666.1:g.6304008_6304018del GRCh37
NC_000004.10:g.6354909_6354919del NCBI36
NG_011700.1:g.37432_37442del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2522_2532del ENSP00000507852.1:p.Leu841ProfsTer?
ENST00000683395.1:c.2463_2473del
ENST00000684087.1:c.2486_2496del ENSP00000506978.1:p.Leu829ProfsTer?
ENST00000506362.2:c.2237_2247del ENSP00000424103.2:p.Leu746ProfsTer?
ENST00000673991.1:c.2522_2532del ENSP00000501033.1:p.Leu841ProfsTer?
ENST00000226760.5:c.2486_2496del MANE Select ENSP00000226760.1:p.Leu829ProfsTer?
ENST00000503569.5:c.2486_2496del ENSP00000423337.1:p.Leu829ProfsTer?
ENST00000507765.1:n.2671_2681del
NM_001145853.1:c.2486_2496del NP_001139325.1:p.Leu829ProfsTer?
NM_006005.3:c.2486_2496del MANE Select NP_005996.2:p.Leu829ProfsTer?
XM_017008586.1:c.2495_2505del XP_016864075.1:p.Leu832ProfsTer?