Canonical Allele Identifier: CA2325780464

Gene: ANKLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283313C= , CM000681.2:g.17283313C=	GRCh38
NC_000019.9:g.17394122C= , CM000681.1:g.17394122C=	GRCh37
NC_000019.8:g.17255122C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404085.7:c.549C= MANE Select	ENSP00000384008.3:p.Gly183=
ENST00000404261.9:c.549C=	ENSP00000384753.6:p.Gly183=
ENST00000594072.6:c.549C=	ENSP00000468845.4:p.Gly183=
ENST00000651416.1:n.766C=
ENST00000652132.1:c.516C=	ENSP00000498416.1:p.Gly172=
ENST00000394458.7:c.711C=	ENSP00000377971.4:p.Gly237=
ENST00000404085.5:c.*448C=	ENSP00000384008.2:n.*448C=
ENST00000404261.8:c.711C=	ENSP00000384753.5:p.Gly237=
ENST00000594072.5:c.711C=	ENSP00000468845.3:p.Gly237=
ENST00000596626.1:n.662C=
ENST00000598347.2:c.551C=
NM_001278443.1:c.678C=	NP_001265372.1:p.Gly226=
NM_001278444.1:c.711C=	NP_001265373.1:p.Gly237=
NM_001278445.1:c.615C=	NP_001265374.1:p.Gly205=
NM_152363.5:c.711C=	NP_689576.5:p.Gly237=
NR_103530.1:n.825C=
NM_001278443.2:c.516C=	NP_001265372.2:p.Gly172=
NM_001278444.2:c.549C=	NP_001265373.2:p.Gly183=
NM_001278445.2:c.507C=	NP_001265374.2:p.Gly169=
NM_152363.6:c.549C= MANE Select	NP_689576.6:p.Gly183=
NR_103530.2:n.569C=