Canonical Allele Identifier: CA2621415458

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318188-CATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318194_121318196del , CM000674.2:g.121318194_121318196del	GRCh38
NC_000012.11:g.121755997_121755999del , CM000674.1:g.121755997_121755999del	GRCh37
NC_000012.10:g.120240380_120240382del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261819.8:c.1893+86_1893+88del MANE Select	ENSP00000261819.3:n.1893+86_1893+88del
ENST00000261819.7:c.1893+86_1893+88del	ENSP00000261819.3:n.1893+86_1893+88del
ENST00000441917.6:c.1557+86_1557+88del	ENSP00000415061.2:n.1557+86_1557+88del
ENST00000534976.5:n.2625+86_2625+88del
ENST00000535482.1:c.891+86_891+88del	ENSP00000438754.1:n.891+86_891+88del
ENST00000535641.5:n.2104+86_2104+88del
ENST00000539079.5:c.1217+86_1217+88del
ENST00000541887.5:c.1854+86_1854+88del	ENSP00000439875.1:n.1854+86_1854+88del
ENST00000544314.5:n.1011+86_1011+88del
ENST00000545218.5:n.1064-37_1064-35del
NM_001137559.1:c.1557+86_1557+88del	NP_001131031.1:n.1557+86_1557+88del
NM_016237.4:c.1893+86_1893+88del	NP_057321.2:n.1893+86_1893+88del
XM_005253900.2:c.1854+86_1854+88del	XP_005253957.1:n.1854+86_1854+88del
XM_006719449.1:c.699+86_699+88del	XP_006719512.1:n.699+86_699+88del
NM_001330489.1:c.1854+86_1854+88del	NP_001317418.1:n.1854+86_1854+88del
XM_017019423.2:c.699+86_699+88del	XP_016874912.1:n.699+86_699+88del
XM_017019424.2:c.699+86_699+88del	XP_016874913.1:n.699+86_699+88del
NM_016237.5:c.1893+86_1893+88del MANE Select	NP_057321.2:n.1893+86_1893+88del
NM_001330489.2:c.1854+86_1854+88del	NP_001317418.1:n.1854+86_1854+88del