Canonical Allele Identifier: CA404744971
Gene: ANKLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283423C>A , CM000681.2:g.17283423C>A GRCh38
NC_000019.9:g.17394232C>A , CM000681.1:g.17394232C>A GRCh37
NC_000019.8:g.17255232C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.659C>A MANE Select ENSP00000384008.3:p.Ser220Tyr
ENST00000404261.9:c.659C>A ENSP00000384753.6:p.Ser220Tyr
ENST00000594072.6:c.659C>A ENSP00000468845.4:p.Ser220Tyr
ENST00000651416.1:n.876C>A
ENST00000652132.1:c.626C>A ENSP00000498416.1:p.Ser209Tyr
ENST00000394458.7:c.821C>A ENSP00000377971.4:p.Ser274Tyr
ENST00000404085.5:c.*558C>A ENSP00000384008.2:n.*558C>A
ENST00000404261.8:c.821C>A ENSP00000384753.5:p.Ser274Tyr
ENST00000594072.5:c.821C>A ENSP00000468845.3:p.Ser274Tyr
ENST00000596626.1:n.772C>A
ENST00000598347.2:c.661C>A
NM_001278443.1:c.788C>A NP_001265372.1:p.Ser263Tyr
NM_001278444.1:c.821C>A NP_001265373.1:p.Ser274Tyr
NM_001278445.1:c.725C>A NP_001265374.1:p.Ser242Tyr
NM_152363.5:c.821C>A NP_689576.5:p.Ser274Tyr
NR_103530.1:n.935C>A
NM_001278443.2:c.626C>A NP_001265372.2:p.Ser209Tyr
NM_001278444.2:c.659C>A NP_001265373.2:p.Ser220Tyr
NM_001278445.2:c.617C>A NP_001265374.2:p.Ser206Tyr
NM_152363.6:c.659C>A MANE Select NP_689576.6:p.Ser220Tyr
NR_103530.2:n.679C>A