Canonical Allele Identifier: CA2067835776

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318535A= , CM000674.2:g.121318535A=	GRCh38
NC_000012.11:g.121756338A= , CM000674.1:g.121756338A=	GRCh37
NC_000012.10:g.120240721A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1711T= MANE Select	ENSP00000261819.3:p.Cys571=
ENST00000261819.7:c.1711T=	ENSP00000261819.3:p.Cys571=
ENST00000366333.3:n.923T=
ENST00000441917.6:c.1375T=	ENSP00000415061.2:p.Cys459=
ENST00000534976.5:n.2367T=
ENST00000535482.1:c.709T=	ENSP00000438754.1:p.Cys237=
ENST00000535641.5:n.1922T=
ENST00000539079.5:c.1055T=
ENST00000541887.5:c.1672T=	ENSP00000439875.1:p.Cys558=
ENST00000544314.5:n.829T=
ENST00000545218.5:n.954T=
NM_001137559.1:c.1375T=	NP_001131031.1:p.Cys459=
NM_016237.4:c.1711T=	NP_057321.2:p.Cys571=
XM_005253900.2:c.1672T=	XP_005253957.1:p.Cys558=
XM_006719449.1:c.517T=	XP_006719512.1:p.Cys173=
NM_001330489.1:c.1672T=	NP_001317418.1:p.Cys558=
XM_017019423.2:c.517T=	XP_016874912.1:p.Cys173=
XM_017019424.2:c.517T=	XP_016874913.1:p.Cys173=
NM_016237.5:c.1711T= MANE Select	NP_057321.2:p.Cys571=
NM_001330489.2:c.1672T=	NP_001317418.1:p.Cys558=