Canonical Allele Identifier: CA2583322834
Gene: ANKLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283041G>T , CM000681.2:g.17283041G>T GRCh38
NC_000019.9:g.17393850G>T , CM000681.1:g.17393850G>T GRCh37
NC_000019.8:g.17254850G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.460+39G>T MANE Select ENSP00000384008.3:n.460+39G>T
ENST00000404261.9:c.460+39G>T ENSP00000384753.6:n.460+39G>T
ENST00000594072.6:c.460+39G>T ENSP00000468845.4:n.460+39G>T
ENST00000651416.1:n.677+39G>T
ENST00000652132.1:c.427+39G>T ENSP00000498416.1:n.427+39G>T
ENST00000394458.7:c.622+39G>T ENSP00000377971.4:n.622+39G>T
ENST00000404085.5:c.*359+39G>T ENSP00000384008.2:n.*359+39G>T
ENST00000404261.8:c.622+39G>T ENSP00000384753.5:n.622+39G>T
ENST00000594072.5:c.622+39G>T ENSP00000468845.3:n.622+39G>T
ENST00000596099.1:n.400G>T
ENST00000596626.1:n.573+39G>T
ENST00000596834.1:n.547G>T
ENST00000598347.2:c.462+39G>T
NM_001278443.1:c.589+39G>T NP_001265372.1:n.589+39G>T
NM_001278444.1:c.622+39G>T NP_001265373.1:n.622+39G>T
NM_001278445.1:c.526+39G>T NP_001265374.1:n.526+39G>T
NM_152363.5:c.622+39G>T NP_689576.5:n.622+39G>T
NR_103530.1:n.736+39G>T
NM_001278443.2:c.427+39G>T NP_001265372.2:n.427+39G>T
NM_001278444.2:c.460+39G>T NP_001265373.2:n.460+39G>T
NM_001278445.2:c.418+39G>T NP_001265374.2:n.418+39G>T
NM_152363.6:c.460+39G>T MANE Select NP_689576.6:n.460+39G>T
NR_103530.2:n.480+39G>T