Canonical Allele Identifier: CA404744892
Gene: ANKLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283387C>T , CM000681.2:g.17283387C>T GRCh38
NC_000019.9:g.17394196C>T , CM000681.1:g.17394196C>T GRCh37
NC_000019.8:g.17255196C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.623C>T MANE Select ENSP00000384008.3:p.Ser208Phe
ENST00000404261.9:c.623C>T ENSP00000384753.6:p.Ser208Phe
ENST00000594072.6:c.623C>T ENSP00000468845.4:p.Ser208Phe
ENST00000651416.1:n.840C>T
ENST00000652132.1:c.590C>T ENSP00000498416.1:p.Ser197Phe
ENST00000394458.7:c.785C>T ENSP00000377971.4:p.Ser262Phe
ENST00000404085.5:c.*522C>T ENSP00000384008.2:n.*522C>T
ENST00000404261.8:c.785C>T ENSP00000384753.5:p.Ser262Phe
ENST00000594072.5:c.785C>T ENSP00000468845.3:p.Ser262Phe
ENST00000596626.1:n.736C>T
ENST00000598347.2:c.625C>T
NM_001278443.1:c.752C>T NP_001265372.1:p.Ser251Phe
NM_001278444.1:c.785C>T NP_001265373.1:p.Ser262Phe
NM_001278445.1:c.689C>T NP_001265374.1:p.Ser230Phe
NM_152363.5:c.785C>T NP_689576.5:p.Ser262Phe
NR_103530.1:n.899C>T
NM_001278443.2:c.590C>T NP_001265372.2:p.Ser197Phe
NM_001278444.2:c.623C>T NP_001265373.2:p.Ser208Phe
NM_001278445.2:c.581C>T NP_001265374.2:p.Ser194Phe
NM_152363.6:c.623C>T MANE Select NP_689576.6:p.Ser208Phe
NR_103530.2:n.643C>T