Canonical Allele Identifier: CA2067835528

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318408C= , CM000674.2:g.121318408C=	GRCh38
NC_000012.11:g.121756211C= , CM000674.1:g.121756211C=	GRCh37
NC_000012.10:g.120240594C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1762G= MANE Select	ENSP00000261819.3:p.Ala588=
ENST00000261819.7:c.1762G=	ENSP00000261819.3:p.Ala588=
ENST00000441917.6:c.1426G=	ENSP00000415061.2:p.Ala476=
ENST00000534976.5:n.2494G=
ENST00000535482.1:c.760G=	ENSP00000438754.1:p.Ala254=
ENST00000535641.5:n.1973G=
ENST00000539079.5:c.1090-4G=
ENST00000541887.5:c.1723G=	ENSP00000439875.1:p.Ala575=
ENST00000544314.5:n.880G=
ENST00000545218.5:n.989-57G=
NM_001137559.1:c.1426G=	NP_001131031.1:p.Ala476=
NM_016237.4:c.1762G=	NP_057321.2:p.Ala588=
XM_005253900.2:c.1723G=	XP_005253957.1:p.Ala575=
XM_006719449.1:c.568G=	XP_006719512.1:p.Ala190=
NM_001330489.1:c.1723G=	NP_001317418.1:p.Ala575=
XM_017019423.2:c.568G=	XP_016874912.1:p.Ala190=
XM_017019424.2:c.568G=	XP_016874913.1:p.Ala190=
NM_016237.5:c.1762G= MANE Select	NP_057321.2:p.Ala588=
NM_001330489.2:c.1723G=	NP_001317418.1:p.Ala575=