Canonical Allele Identifier: CA2621415632

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318482-T-TGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318484_121318485insGGT , CM000674.2:g.121318484_121318485insGGT	GRCh38
NC_000012.11:g.121756287_121756288insGGT , CM000674.1:g.121756287_121756288insGGT	GRCh37
NC_000012.10:g.120240670_120240671insGGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1745+18_1745+19insCAC MANE Select	ENSP00000261819.3:n.1745+18_1745+19insCAC
ENST00000261819.7:c.1745+18_1745+19insCAC	ENSP00000261819.3:n.1745+18_1745+19insCAC
ENST00000441917.6:c.1409+18_1409+19insCAC	ENSP00000415061.2:n.1409+18_1409+19insCAC
ENST00000534976.5:n.2419_2420insCAC
ENST00000535482.1:c.743+18_743+19insCAC	ENSP00000438754.1:n.743+18_743+19insCAC
ENST00000535641.5:n.1956+18_1956+19insCAC
ENST00000539079.5:c.1089+18_1089+19insCAC
ENST00000541887.5:c.1706+18_1706+19insCAC	ENSP00000439875.1:n.1706+18_1706+19insCAC
ENST00000544314.5:n.863+18_863+19insCAC
ENST00000545218.5:n.988+18_988+19insCAC
NM_001137559.1:c.1409+18_1409+19insCAC	NP_001131031.1:n.1409+18_1409+19insCAC
NM_016237.4:c.1745+18_1745+19insCAC	NP_057321.2:n.1745+18_1745+19insCAC
XM_005253900.2:c.1706+18_1706+19insCAC	XP_005253957.1:n.1706+18_1706+19insCAC
XM_006719449.1:c.551+18_551+19insCAC	XP_006719512.1:n.551+18_551+19insCAC
NM_001330489.1:c.1706+18_1706+19insCAC	NP_001317418.1:n.1706+18_1706+19insCAC
XM_017019423.2:c.551+18_551+19insCAC	XP_016874912.1:n.551+18_551+19insCAC
XM_017019424.2:c.551+18_551+19insCAC	XP_016874913.1:n.551+18_551+19insCAC
NM_016237.5:c.1745+18_1745+19insCAC MANE Select	NP_057321.2:n.1745+18_1745+19insCAC
NM_001330489.2:c.1706+18_1706+19insCAC	NP_001317418.1:n.1706+18_1706+19insCAC