Canonical Allele Identifier: CA2067835771

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318532G= , CM000674.2:g.121318532G=	GRCh38
NC_000012.11:g.121756335G= , CM000674.1:g.121756335G=	GRCh37
NC_000012.10:g.120240718G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1714C= MANE Select	ENSP00000261819.3:p.Gln572=
ENST00000261819.7:c.1714C=	ENSP00000261819.3:p.Gln572=
ENST00000441917.6:c.1378C=	ENSP00000415061.2:p.Gln460=
ENST00000534976.5:n.2370C=
ENST00000535482.1:c.712C=	ENSP00000438754.1:p.Gln238=
ENST00000535641.5:n.1925C=
ENST00000539079.5:c.1058C=
ENST00000541887.5:c.1675C=	ENSP00000439875.1:p.Gln559=
ENST00000544314.5:n.832C=
ENST00000545218.5:n.957C=
NM_001137559.1:c.1378C=	NP_001131031.1:p.Gln460=
NM_016237.4:c.1714C=	NP_057321.2:p.Gln572=
XM_005253900.2:c.1675C=	XP_005253957.1:p.Gln559=
XM_006719449.1:c.520C=	XP_006719512.1:p.Gln174=
NM_001330489.1:c.1675C=	NP_001317418.1:p.Gln559=
XM_017019423.2:c.520C=	XP_016874912.1:p.Gln174=
XM_017019424.2:c.520C=	XP_016874913.1:p.Gln174=
NM_016237.5:c.1714C= MANE Select	NP_057321.2:p.Gln572=
NM_001330489.2:c.1675C=	NP_001317418.1:p.Gln559=