Canonical Allele Identifier: CA404744560

Gene: ANKLE1

Linked Data

• MyVariant Identifiers: chr19:g.17394034C>G (hg19) ; chr19:g.17283225C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283225C>G , CM000681.2:g.17283225C>G	GRCh38
NC_000019.9:g.17394034C>G , CM000681.1:g.17394034C>G	GRCh37
NC_000019.8:g.17255034C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404085.7:c.461C>G MANE Select	ENSP00000384008.3:p.Thr154Ser
ENST00000404261.9:c.461C>G	ENSP00000384753.6:p.Thr154Ser
ENST00000594072.6:c.461C>G	ENSP00000468845.4:p.Thr154Ser
ENST00000651416.1:n.678C>G
ENST00000652132.1:c.428C>G	ENSP00000498416.1:p.Thr143Ser
ENST00000394458.7:c.623C>G	ENSP00000377971.4:p.Thr208Ser
ENST00000404085.5:c.*360C>G	ENSP00000384008.2:n.*360C>G
ENST00000404261.8:c.623C>G	ENSP00000384753.5:p.Thr208Ser
ENST00000594072.5:c.623C>G	ENSP00000468845.3:p.Thr208Ser
ENST00000596626.1:n.574C>G
ENST00000598347.2:c.463C>G
NM_001278443.1:c.590C>G	NP_001265372.1:p.Thr197Ser
NM_001278444.1:c.623C>G	NP_001265373.1:p.Thr208Ser
NM_001278445.1:c.527C>G	NP_001265374.1:p.Thr176Ser
NM_152363.5:c.623C>G	NP_689576.5:p.Thr208Ser
NR_103530.1:n.737C>G
NM_001278443.2:c.428C>G	NP_001265372.2:p.Thr143Ser
NM_001278444.2:c.461C>G	NP_001265373.2:p.Thr154Ser
NM_001278445.2:c.419C>G	NP_001265374.2:p.Thr140Ser
NM_152363.6:c.461C>G MANE Select	NP_689576.6:p.Thr154Ser
NR_103530.2:n.481C>G