Canonical Allele Identifier: CA2067835625

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318482T= , CM000674.2:g.121318482T=	GRCh38
NC_000012.11:g.121756285T= , CM000674.1:g.121756285T=	GRCh37
NC_000012.10:g.120240668T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1745+19A= MANE Select	ENSP00000261819.3:n.1745+19A=
ENST00000261819.7:c.1745+19A=	ENSP00000261819.3:n.1745+19A=
ENST00000441917.6:c.1409+19A=	ENSP00000415061.2:n.1409+19A=
ENST00000534976.5:n.2420A=
ENST00000535482.1:c.743+19A=	ENSP00000438754.1:n.743+19A=
ENST00000535641.5:n.1956+19A=
ENST00000539079.5:c.1089+19A=
ENST00000541887.5:c.1706+19A=	ENSP00000439875.1:n.1706+19A=
ENST00000544314.5:n.863+19A=
ENST00000545218.5:n.988+19A=
NM_001137559.1:c.1409+19A=	NP_001131031.1:n.1409+19A=
NM_016237.4:c.1745+19A=	NP_057321.2:n.1745+19A=
XM_005253900.2:c.1706+19A=	XP_005253957.1:n.1706+19A=
XM_006719449.1:c.551+19A=	XP_006719512.1:n.551+19A=
NM_001330489.1:c.1706+19A=	NP_001317418.1:n.1706+19A=
XM_017019423.2:c.551+19A=	XP_016874912.1:n.551+19A=
XM_017019424.2:c.551+19A=	XP_016874913.1:n.551+19A=
NM_016237.5:c.1745+19A= MANE Select	NP_057321.2:n.1745+19A=
NM_001330489.2:c.1706+19A=	NP_001317418.1:n.1706+19A=