Canonical Allele Identifier: CA404744756
Gene: ANKLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17283318A>C , CM000681.2:g.17283318A>C GRCh38
NC_000019.9:g.17394127A>C , CM000681.1:g.17394127A>C GRCh37
NC_000019.8:g.17255127A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000404085.7:c.554A>C MANE Select ENSP00000384008.3:p.Glu185Ala
ENST00000404261.9:c.554A>C ENSP00000384753.6:p.Glu185Ala
ENST00000594072.6:c.554A>C ENSP00000468845.4:p.Glu185Ala
ENST00000651416.1:n.771A>C
ENST00000652132.1:c.521A>C ENSP00000498416.1:p.Glu174Ala
ENST00000394458.7:c.716A>C ENSP00000377971.4:p.Glu239Ala
ENST00000404085.5:c.*453A>C ENSP00000384008.2:n.*453A>C
ENST00000404261.8:c.716A>C ENSP00000384753.5:p.Glu239Ala
ENST00000594072.5:c.716A>C ENSP00000468845.3:p.Glu239Ala
ENST00000596626.1:n.667A>C
ENST00000598347.2:c.556A>C
NM_001278443.1:c.683A>C NP_001265372.1:p.Glu228Ala
NM_001278444.1:c.716A>C NP_001265373.1:p.Glu239Ala
NM_001278445.1:c.620A>C NP_001265374.1:p.Glu207Ala
NM_152363.5:c.716A>C NP_689576.5:p.Glu239Ala
NR_103530.1:n.830A>C
NM_001278443.2:c.521A>C NP_001265372.2:p.Glu174Ala
NM_001278444.2:c.554A>C NP_001265373.2:p.Glu185Ala
NM_001278445.2:c.512A>C NP_001265374.2:p.Glu171Ala
NM_152363.6:c.554A>C MANE Select NP_689576.6:p.Glu185Ala
NR_103530.2:n.574A>C