Canonical Allele Identifier: CA2067835805

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318564T= , CM000674.2:g.121318564T=	GRCh38
NC_000012.11:g.121756367T= , CM000674.1:g.121756367T=	GRCh37
NC_000012.10:g.120240750T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1682A= MANE Select	ENSP00000261819.3:p.His561=
ENST00000261819.7:c.1682A=	ENSP00000261819.3:p.His561=
ENST00000366333.3:n.894A=
ENST00000441917.6:c.1346A=	ENSP00000415061.2:p.His449=
ENST00000534976.5:n.2338A=
ENST00000535482.1:c.680A=	ENSP00000438754.1:p.His227=
ENST00000535641.5:n.1893A=
ENST00000539079.5:c.1026A=
ENST00000541887.5:c.1643A=	ENSP00000439875.1:p.His548=
ENST00000544314.5:n.800A=
ENST00000545218.5:n.925A=
NM_001137559.1:c.1346A=	NP_001131031.1:p.His449=
NM_016237.4:c.1682A=	NP_057321.2:p.His561=
XM_005253900.2:c.1643A=	XP_005253957.1:p.His548=
XM_006719449.1:c.488A=	XP_006719512.1:p.His163=
NM_001330489.1:c.1643A=	NP_001317418.1:p.His548=
XM_017019423.2:c.488A=	XP_016874912.1:p.His163=
XM_017019424.2:c.488A=	XP_016874913.1:p.His163=
NM_016237.5:c.1682A= MANE Select	NP_057321.2:p.His561=
NM_001330489.2:c.1643A=	NP_001317418.1:p.His548=