Canonical Allele Identifier: CA404744759
Gene: ANKLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283320G>C , CM000681.2:g.17283320G>C GRCh38
NC_000019.9:g.17394129G>C , CM000681.1:g.17394129G>C GRCh37
NC_000019.8:g.17255129G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000404085.7:c.556G>C MANE Select ENSP00000384008.3:p.Ala186Pro
ENST00000404261.9:c.556G>C ENSP00000384753.6:p.Ala186Pro
ENST00000594072.6:c.556G>C ENSP00000468845.4:p.Ala186Pro
ENST00000651416.1:n.773G>C
ENST00000652132.1:c.523G>C ENSP00000498416.1:p.Ala175Pro
ENST00000394458.7:c.718G>C ENSP00000377971.4:p.Ala240Pro
ENST00000404085.5:c.*455G>C ENSP00000384008.2:n.*455G>C
ENST00000404261.8:c.718G>C ENSP00000384753.5:p.Ala240Pro
ENST00000594072.5:c.718G>C ENSP00000468845.3:p.Ala240Pro
ENST00000596626.1:n.669G>C
ENST00000598347.2:c.558G>C
NM_001278443.1:c.685G>C NP_001265372.1:p.Ala229Pro
NM_001278444.1:c.718G>C NP_001265373.1:p.Ala240Pro
NM_001278445.1:c.622G>C NP_001265374.1:p.Ala208Pro
NM_152363.5:c.718G>C NP_689576.5:p.Ala240Pro
NR_103530.1:n.832G>C
NM_001278443.2:c.523G>C NP_001265372.2:p.Ala175Pro
NM_001278444.2:c.556G>C NP_001265373.2:p.Ala186Pro
NM_001278445.2:c.514G>C NP_001265374.2:p.Ala172Pro
NM_152363.6:c.556G>C MANE Select NP_689576.6:p.Ala186Pro
NR_103530.2:n.576G>C