Canonical Allele Identifier: CA2840306457
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301033dup , CM000666.2:g.6301033dup GRCh38
NC_000004.11:g.6302760dup , CM000666.1:g.6302760dup GRCh37
NC_000004.10:g.6353661dup NCBI36
NG_011700.1:g.36184dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1274dup ENSP00000507852.1:p.Phe426LeufsTer?
ENST00000683395.1:c.1215dup
ENST00000684087.1:c.1238dup ENSP00000506978.1:p.Phe414LeufsTer?
ENST00000506362.2:c.989dup ENSP00000424103.2:p.Phe331LeufsTer?
ENST00000673642.1:c.897dup ENSP00000501242.1:p.Leu300SerfsTer29
ENST00000673991.1:c.1274dup ENSP00000501033.1:p.Phe426LeufsTer?
ENST00000226760.5:c.1238dup MANE Select ENSP00000226760.1:p.Phe414LeufsTer?
ENST00000503569.5:c.1238dup ENSP00000423337.1:p.Phe414LeufsTer?
ENST00000507765.1:n.1423dup
NM_001145853.1:c.1238dup NP_001139325.1:p.Phe414LeufsTer?
NM_006005.3:c.1238dup MANE Select NP_005996.2:p.Phe414LeufsTer?
XM_017008586.1:c.1247dup XP_016864075.1:p.Phe417LeufsTer?