Canonical Allele Identifier: CA2325780400
Gene: ANKLE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283183A= , CM000681.2:g.17283183A= GRCh38
NC_000019.9:g.17393992A= , CM000681.1:g.17393992A= GRCh37
NC_000019.8:g.17254992A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.461-42A= MANE Select ENSP00000384008.3:n.461-42A=
ENST00000404261.9:c.461-42A= ENSP00000384753.6:n.461-42A=
ENST00000594072.6:c.461-42A= ENSP00000468845.4:n.461-42A=
ENST00000651416.1:n.678-42A=
ENST00000652132.1:c.428-42A= ENSP00000498416.1:n.428-42A=
ENST00000394458.7:c.623-42A= ENSP00000377971.4:n.623-42A=
ENST00000404085.5:c.*360-42A= ENSP00000384008.2:n.*360-42A=
ENST00000404261.8:c.623-42A= ENSP00000384753.5:n.623-42A=
ENST00000594072.5:c.623-42A= ENSP00000468845.3:n.623-42A=
ENST00000596626.1:n.574-42A=
ENST00000598347.2:c.463-42A=
NM_001278443.1:c.590-42A= NP_001265372.1:n.590-42A=
NM_001278444.1:c.623-42A= NP_001265373.1:n.623-42A=
NM_001278445.1:c.527-42A= NP_001265374.1:n.527-42A=
NM_152363.5:c.623-42A= NP_689576.5:n.623-42A=
NR_103530.1:n.737-42A=
NM_001278443.2:c.428-42A= NP_001265372.2:n.428-42A=
NM_001278444.2:c.461-42A= NP_001265373.2:n.461-42A=
NM_001278445.2:c.419-42A= NP_001265374.2:n.419-42A=
NM_152363.6:c.461-42A= MANE Select NP_689576.6:n.461-42A=
NR_103530.2:n.481-42A=