Canonical Allele Identifier: CA2586973656
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302300dup , CM000666.2:g.6302300dup GRCh38
NC_000004.11:g.6304027dup , CM000666.1:g.6304027dup GRCh37
NC_000004.10:g.6354928dup NCBI36
NG_011700.1:g.37451dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2541dup ENSP00000507852.1:p.Lys848GlnfsTer?
ENST00000683395.1:c.2482dup
ENST00000684087.1:c.2505dup ENSP00000506978.1:p.Lys836GlnfsTer?
ENST00000506362.2:c.2256dup ENSP00000424103.2:p.Lys753GlnfsTer?
ENST00000673991.1:c.2541dup ENSP00000501033.1:p.Lys848GlnfsTer?
ENST00000226760.5:c.2505dup MANE Select ENSP00000226760.1:p.Lys836GlnfsTer?
ENST00000503569.5:c.2505dup ENSP00000423337.1:p.Lys836GlnfsTer?
ENST00000507765.1:n.2690dup
NM_001145853.1:c.2505dup NP_001139325.1:p.Lys836GlnfsTer?
NM_006005.3:c.2505dup MANE Select NP_005996.2:p.Lys836GlnfsTer?
XM_017008586.1:c.2514dup XP_016864075.1:p.Lys839GlnfsTer?