Canonical Allele Identifier: CA2325780366
Gene: ANKLE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283108A= , CM000681.2:g.17283108A= GRCh38
NC_000019.9:g.17393917A= , CM000681.1:g.17393917A= GRCh37
NC_000019.8:g.17254917A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.460+106A= MANE Select ENSP00000384008.3:n.460+106A=
ENST00000404261.9:c.460+106A= ENSP00000384753.6:n.460+106A=
ENST00000594072.6:c.460+106A= ENSP00000468845.4:n.460+106A=
ENST00000651416.1:n.677+106A=
ENST00000652132.1:c.427+106A= ENSP00000498416.1:n.427+106A=
ENST00000394458.7:c.622+106A= ENSP00000377971.4:n.622+106A=
ENST00000404085.5:c.*359+106A= ENSP00000384008.2:n.*359+106A=
ENST00000404261.8:c.622+106A= ENSP00000384753.5:n.622+106A=
ENST00000594072.5:c.622+106A= ENSP00000468845.3:n.622+106A=
ENST00000596099.1:n.467A=
ENST00000596626.1:n.573+106A=
ENST00000598347.2:c.462+106A=
NM_001278443.1:c.589+106A= NP_001265372.1:n.589+106A=
NM_001278444.1:c.622+106A= NP_001265373.1:n.622+106A=
NM_001278445.1:c.526+106A= NP_001265374.1:n.526+106A=
NM_152363.5:c.622+106A= NP_689576.5:n.622+106A=
NR_103530.1:n.736+106A=
NM_001278443.2:c.427+106A= NP_001265372.2:n.427+106A=
NM_001278444.2:c.460+106A= NP_001265373.2:n.460+106A=
NM_001278445.2:c.418+106A= NP_001265374.2:n.418+106A=
NM_152363.6:c.460+106A= MANE Select NP_689576.6:n.460+106A=
NR_103530.2:n.480+106A=