Canonical Allele Identifier: CA306086205

Gene: ANKLE1

Linked Data

• dbSNP Id: rs1006489021
• MyVariant Identifiers: chr19:g.17394129G>A (hg19) ; chr19:g.17283320G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283320G>A , CM000681.2:g.17283320G>A	GRCh38
NC_000019.9:g.17394129G>A , CM000681.1:g.17394129G>A	GRCh37
NC_000019.8:g.17255129G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000404085.7:c.556G>A MANE Select	ENSP00000384008.3:p.Ala186Thr
ENST00000404261.9:c.556G>A	ENSP00000384753.6:p.Ala186Thr
ENST00000594072.6:c.556G>A	ENSP00000468845.4:p.Ala186Thr
ENST00000651416.1:n.773G>A
ENST00000652132.1:c.523G>A	ENSP00000498416.1:p.Ala175Thr
ENST00000394458.7:c.718G>A	ENSP00000377971.4:p.Ala240Thr
ENST00000404085.5:c.*455G>A	ENSP00000384008.2:n.*455G>A
ENST00000404261.8:c.718G>A	ENSP00000384753.5:p.Ala240Thr
ENST00000594072.5:c.718G>A	ENSP00000468845.3:p.Ala240Thr
ENST00000596626.1:n.669G>A
ENST00000598347.2:c.558G>A
NM_001278443.1:c.685G>A	NP_001265372.1:p.Ala229Thr
NM_001278444.1:c.718G>A	NP_001265373.1:p.Ala240Thr
NM_001278445.1:c.622G>A	NP_001265374.1:p.Ala208Thr
NM_152363.5:c.718G>A	NP_689576.5:p.Ala240Thr
NR_103530.1:n.832G>A
NM_001278443.2:c.523G>A	NP_001265372.2:p.Ala175Thr
NM_001278444.2:c.556G>A	NP_001265373.2:p.Ala186Thr
NM_001278445.2:c.514G>A	NP_001265374.2:p.Ala172Thr
NM_152363.6:c.556G>A MANE Select	NP_689576.6:p.Ala186Thr
NR_103530.2:n.576G>A