Canonical Allele Identifier: CA2067835251

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318319C= , CM000674.2:g.121318319C=	GRCh38
NC_000012.11:g.121756122C= , CM000674.1:g.121756122C=	GRCh37
NC_000012.10:g.120240505C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1851G= MANE Select	ENSP00000261819.3:p.Gln617=
ENST00000261819.7:c.1851G=	ENSP00000261819.3:p.Gln617=
ENST00000441917.6:c.1515G=	ENSP00000415061.2:p.Gln505=
ENST00000534976.5:n.2583G=
ENST00000535482.1:c.849G=	ENSP00000438754.1:p.Gln283=
ENST00000535641.5:n.2062G=
ENST00000539079.5:c.1175G=
ENST00000541887.5:c.1812G=	ENSP00000439875.1:p.Gln604=
ENST00000544314.5:n.969G=
ENST00000545218.5:n.1021G=
NM_001137559.1:c.1515G=	NP_001131031.1:p.Gln505=
NM_016237.4:c.1851G=	NP_057321.2:p.Gln617=
XM_005253900.2:c.1812G=	XP_005253957.1:p.Gln604=
XM_006719449.1:c.657G=	XP_006719512.1:p.Gln219=
NM_001330489.1:c.1812G=	NP_001317418.1:p.Gln604=
XM_017019423.2:c.657G=	XP_016874912.1:p.Gln219=
XM_017019424.2:c.657G=	XP_016874913.1:p.Gln219=
NM_016237.5:c.1851G= MANE Select	NP_057321.2:p.Gln617=
NM_001330489.2:c.1812G=	NP_001317418.1:p.Gln604=