Canonical Allele Identifier: CA2325780323

Gene: ANKLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283031C= , CM000681.2:g.17283031C=	GRCh38
NC_000019.9:g.17393840C= , CM000681.1:g.17393840C=	GRCh37
NC_000019.8:g.17254840C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404085.7:c.460+29C= MANE Select	ENSP00000384008.3:n.460+29C=
ENST00000404261.9:c.460+29C=	ENSP00000384753.6:n.460+29C=
ENST00000594072.6:c.460+29C=	ENSP00000468845.4:n.460+29C=
ENST00000651416.1:n.677+29C=
ENST00000652132.1:c.427+29C=	ENSP00000498416.1:n.427+29C=
ENST00000394458.7:c.622+29C=	ENSP00000377971.4:n.622+29C=
ENST00000404085.5:c.*359+29C=	ENSP00000384008.2:n.*359+29C=
ENST00000404261.8:c.622+29C=	ENSP00000384753.5:n.622+29C=
ENST00000594072.5:c.622+29C=	ENSP00000468845.3:n.622+29C=
ENST00000596099.1:n.390C=
ENST00000596626.1:n.573+29C=
ENST00000596834.1:n.537C=
ENST00000598347.2:c.462+29C=
NM_001278443.1:c.589+29C=	NP_001265372.1:n.589+29C=
NM_001278444.1:c.622+29C=	NP_001265373.1:n.622+29C=
NM_001278445.1:c.526+29C=	NP_001265374.1:n.526+29C=
NM_152363.5:c.622+29C=	NP_689576.5:n.622+29C=
NR_103530.1:n.736+29C=
NM_001278443.2:c.427+29C=	NP_001265372.2:n.427+29C=
NM_001278444.2:c.460+29C=	NP_001265373.2:n.460+29C=
NM_001278445.2:c.418+29C=	NP_001265374.2:n.418+29C=
NM_152363.6:c.460+29C= MANE Select	NP_689576.6:n.460+29C=
NR_103530.2:n.480+29C=