Canonical Allele Identifier: CA404744973
Gene: ANKLE1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.659C>G MANE Select ENSP00000384008.3:p.Ser220Cys
ENST00000404261.9:c.659C>G ENSP00000384753.6:p.Ser220Cys
ENST00000594072.6:c.659C>G ENSP00000468845.4:p.Ser220Cys
ENST00000651416.1:n.876C>G
ENST00000652132.1:c.626C>G ENSP00000498416.1:p.Ser209Cys
ENST00000394458.7:c.821C>G ENSP00000377971.4:p.Ser274Cys
ENST00000404085.5:c.*558C>G ENSP00000384008.2:n.*558C>G
ENST00000404261.8:c.821C>G ENSP00000384753.5:p.Ser274Cys
ENST00000594072.5:c.821C>G ENSP00000468845.3:p.Ser274Cys
ENST00000596626.1:n.772C>G
ENST00000598347.2:c.661C>G
NM_001278443.1:c.788C>G NP_001265372.1:p.Ser263Cys
NM_001278444.1:c.821C>G NP_001265373.1:p.Ser274Cys
NM_001278445.1:c.725C>G NP_001265374.1:p.Ser242Cys
NM_152363.5:c.821C>G NP_689576.5:p.Ser274Cys
NR_103530.1:n.935C>G
NM_001278443.2:c.626C>G NP_001265372.2:p.Ser209Cys
NM_001278444.2:c.659C>G NP_001265373.2:p.Ser220Cys
NM_001278445.2:c.617C>G NP_001265374.2:p.Ser206Cys
NM_152363.6:c.659C>G MANE Select NP_689576.6:p.Ser220Cys
NR_103530.2:n.679C>G