Canonical Allele Identifier: CA404744885

Gene: ANKLE1

Linked Data

• MyVariant Identifiers: chr19:g.17394192G>C (hg19) ; chr19:g.17283383G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283383G>C , CM000681.2:g.17283383G>C	GRCh38
NC_000019.9:g.17394192G>C , CM000681.1:g.17394192G>C	GRCh37
NC_000019.8:g.17255192G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404085.7:c.619G>C MANE Select	ENSP00000384008.3:p.Ala207Pro
ENST00000404261.9:c.619G>C	ENSP00000384753.6:p.Ala207Pro
ENST00000594072.6:c.619G>C	ENSP00000468845.4:p.Ala207Pro
ENST00000651416.1:n.836G>C
ENST00000652132.1:c.586G>C	ENSP00000498416.1:p.Ala196Pro
ENST00000394458.7:c.781G>C	ENSP00000377971.4:p.Ala261Pro
ENST00000404085.5:c.*518G>C	ENSP00000384008.2:n.*518G>C
ENST00000404261.8:c.781G>C	ENSP00000384753.5:p.Ala261Pro
ENST00000594072.5:c.781G>C	ENSP00000468845.3:p.Ala261Pro
ENST00000596626.1:n.732G>C
ENST00000598347.2:c.621G>C
NM_001278443.1:c.748G>C	NP_001265372.1:p.Ala250Pro
NM_001278444.1:c.781G>C	NP_001265373.1:p.Ala261Pro
NM_001278445.1:c.685G>C	NP_001265374.1:p.Ala229Pro
NM_152363.5:c.781G>C	NP_689576.5:p.Ala261Pro
NR_103530.1:n.895G>C
NM_001278443.2:c.586G>C	NP_001265372.2:p.Ala196Pro
NM_001278444.2:c.619G>C	NP_001265373.2:p.Ala207Pro
NM_001278445.2:c.577G>C	NP_001265374.2:p.Ala193Pro
NM_152363.6:c.619G>C MANE Select	NP_689576.6:p.Ala207Pro
NR_103530.2:n.639G>C