Canonical Allele Identifier: CA2797736950

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318489_121318500del , CM000674.2:g.121318489_121318500del	GRCh38
NC_000012.11:g.121756292_121756303del , CM000674.1:g.121756292_121756303del	GRCh37
NC_000012.10:g.120240675_120240686del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1745+1_1745+12del MANE Select	ENSP00000261819.3:n.1745+1_1745+12del
ENST00000261819.7:c.1745+1_1745+12del	ENSP00000261819.3:n.1745+1_1745+12del
ENST00000441917.6:c.1409+1_1409+12del	ENSP00000415061.2:n.1409+1_1409+12del
ENST00000534976.5:n.2402_2413del
ENST00000535482.1:c.743+1_743+12del	ENSP00000438754.1:n.743+1_743+12del
ENST00000535641.5:n.1956+1_1956+12del
ENST00000539079.5:c.1089+1_1089+12del
ENST00000541887.5:c.1706+1_1706+12del	ENSP00000439875.1:n.1706+1_1706+12del
ENST00000544314.5:n.863+1_863+12del
ENST00000545218.5:n.988+1_988+12del
NM_001137559.1:c.1409+1_1409+12del	NP_001131031.1:n.1409+1_1409+12del
NM_016237.4:c.1745+1_1745+12del	NP_057321.2:n.1745+1_1745+12del
XM_005253900.2:c.1706+1_1706+12del	XP_005253957.1:n.1706+1_1706+12del
XM_006719449.1:c.551+1_551+12del	XP_006719512.1:n.551+1_551+12del
NM_001330489.1:c.1706+1_1706+12del	NP_001317418.1:n.1706+1_1706+12del
XM_017019423.2:c.551+1_551+12del	XP_016874912.1:n.551+1_551+12del
XM_017019424.2:c.551+1_551+12del	XP_016874913.1:n.551+1_551+12del
NM_016237.5:c.1745+1_1745+12del MANE Select	NP_057321.2:n.1745+1_1745+12del
NM_001330489.2:c.1706+1_1706+12del	NP_001317418.1:n.1706+1_1706+12del