Canonical Allele Identifier: CA2325780456

Gene: ANKLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283294G= , CM000681.2:g.17283294G=	GRCh38
NC_000019.9:g.17394103G= , CM000681.1:g.17394103G=	GRCh37
NC_000019.8:g.17255103G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404085.7:c.530G= MANE Select	ENSP00000384008.3:p.Gly177=
ENST00000404261.9:c.530G=	ENSP00000384753.6:p.Gly177=
ENST00000594072.6:c.530G=	ENSP00000468845.4:p.Gly177=
ENST00000651416.1:n.747G=
ENST00000652132.1:c.497G=	ENSP00000498416.1:p.Gly166=
ENST00000394458.7:c.692G=	ENSP00000377971.4:p.Gly231=
ENST00000404085.5:c.*429G=	ENSP00000384008.2:n.*429G=
ENST00000404261.8:c.692G=	ENSP00000384753.5:p.Gly231=
ENST00000594072.5:c.692G=	ENSP00000468845.3:p.Gly231=
ENST00000596626.1:n.643G=
ENST00000598347.2:c.532G=
NM_001278443.1:c.659G=	NP_001265372.1:p.Gly220=
NM_001278444.1:c.692G=	NP_001265373.1:p.Gly231=
NM_001278445.1:c.596G=	NP_001265374.1:p.Gly199=
NM_152363.5:c.692G=	NP_689576.5:p.Gly231=
NR_103530.1:n.806G=
NM_001278443.2:c.497G=	NP_001265372.2:p.Gly166=
NM_001278444.2:c.530G=	NP_001265373.2:p.Gly177=
NM_001278445.2:c.488G=	NP_001265374.2:p.Gly163=
NM_152363.6:c.530G= MANE Select	NP_689576.6:p.Gly177=
NR_103530.2:n.550G=