Canonical Allele Identifier: CA2325780474

Gene: ANKLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283326C= , CM000681.2:g.17283326C=	GRCh38
NC_000019.9:g.17394135C= , CM000681.1:g.17394135C=	GRCh37
NC_000019.8:g.17255135C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000404085.7:c.562C= MANE Select	ENSP00000384008.3:p.Pro188=
ENST00000404261.9:c.562C=	ENSP00000384753.6:p.Pro188=
ENST00000594072.6:c.562C=	ENSP00000468845.4:p.Pro188=
ENST00000651416.1:n.779C=
ENST00000652132.1:c.529C=	ENSP00000498416.1:p.Pro177=
ENST00000394458.7:c.724C=	ENSP00000377971.4:p.Pro242=
ENST00000404085.5:c.*461C=	ENSP00000384008.2:n.*461C=
ENST00000404261.8:c.724C=	ENSP00000384753.5:p.Pro242=
ENST00000594072.5:c.724C=	ENSP00000468845.3:p.Pro242=
ENST00000596626.1:n.675C=
ENST00000598347.2:c.564C=
NM_001278443.1:c.691C=	NP_001265372.1:p.Pro231=
NM_001278444.1:c.724C=	NP_001265373.1:p.Pro242=
NM_001278445.1:c.628C=	NP_001265374.1:p.Pro210=
NM_152363.5:c.724C=	NP_689576.5:p.Pro242=
NR_103530.1:n.838C=
NM_001278443.2:c.529C=	NP_001265372.2:p.Pro177=
NM_001278444.2:c.562C=	NP_001265373.2:p.Pro188=
NM_001278445.2:c.520C=	NP_001265374.2:p.Pro174=
NM_152363.6:c.562C= MANE Select	NP_689576.6:p.Pro188=
NR_103530.2:n.582C=