Canonical Allele Identifier: CA2325780320
Gene: ANKLE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283019G= , CM000681.2:g.17283019G= GRCh38
NC_000019.9:g.17393828G= , CM000681.1:g.17393828G= GRCh37
NC_000019.8:g.17254828G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.460+17G= MANE Select ENSP00000384008.3:n.460+17G=
ENST00000404261.9:c.460+17G= ENSP00000384753.6:n.460+17G=
ENST00000594072.6:c.460+17G= ENSP00000468845.4:n.460+17G=
ENST00000651416.1:n.677+17G=
ENST00000652132.1:c.427+17G= ENSP00000498416.1:n.427+17G=
ENST00000394458.7:c.622+17G= ENSP00000377971.4:n.622+17G=
ENST00000404085.5:c.*359+17G= ENSP00000384008.2:n.*359+17G=
ENST00000404261.8:c.622+17G= ENSP00000384753.5:n.622+17G=
ENST00000594072.5:c.622+17G= ENSP00000468845.3:n.622+17G=
ENST00000596099.1:n.378G=
ENST00000596626.1:n.573+17G=
ENST00000596834.1:n.525G=
ENST00000598347.2:c.462+17G=
NM_001278443.1:c.589+17G= NP_001265372.1:n.589+17G=
NM_001278444.1:c.622+17G= NP_001265373.1:n.622+17G=
NM_001278445.1:c.526+17G= NP_001265374.1:n.526+17G=
NM_152363.5:c.622+17G= NP_689576.5:n.622+17G=
NR_103530.1:n.736+17G=
NM_001278443.2:c.427+17G= NP_001265372.2:n.427+17G=
NM_001278444.2:c.460+17G= NP_001265373.2:n.460+17G=
NM_001278445.2:c.418+17G= NP_001265374.2:n.418+17G=
NM_152363.6:c.460+17G= MANE Select NP_689576.6:n.460+17G=
NR_103530.2:n.480+17G=