Canonical Allele Identifier: CA506095612
Gene: ANKLE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17394152C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283343C>T , CM000681.2:g.17283343C>T GRCh38
NC_000019.9:g.17394152C>T , CM000681.1:g.17394152C>T GRCh37
NC_000019.8:g.17255152C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404085.7:c.579C>T MANE Select ENSP00000384008.3:p.Leu193=
ENST00000404261.9:c.579C>T ENSP00000384753.6:p.Leu193=
ENST00000594072.6:c.579C>T ENSP00000468845.4:p.Leu193=
ENST00000651416.1:n.796C>T
ENST00000652132.1:c.546C>T ENSP00000498416.1:p.Leu182=
ENST00000394458.7:c.741C>T ENSP00000377971.4:p.Leu247=
ENST00000404085.5:c.*478C>T ENSP00000384008.2:n.*478C>T
ENST00000404261.8:c.741C>T ENSP00000384753.5:p.Leu247=
ENST00000594072.5:c.741C>T ENSP00000468845.3:p.Leu247=
ENST00000596626.1:n.692C>T
ENST00000598347.2:c.581C>T
NM_001278443.1:c.708C>T NP_001265372.1:p.Leu236=
NM_001278444.1:c.741C>T NP_001265373.1:p.Leu247=
NM_001278445.1:c.645C>T NP_001265374.1:p.Leu215=
NM_152363.5:c.741C>T NP_689576.5:p.Leu247=
NR_103530.1:n.855C>T
NM_001278443.2:c.546C>T NP_001265372.2:p.Leu182=
NM_001278444.2:c.579C>T NP_001265373.2:p.Leu193=
NM_001278445.2:c.537C>T NP_001265374.2:p.Leu179=
NM_152363.6:c.579C>T MANE Select NP_689576.6:p.Leu193=
NR_103530.2:n.599C>T