Canonical Allele Identifier: CA386960599

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318505-T-C
• MyVariant Identifiers: chr12:g.121756308T>C (hg19) ; chr12:g.121318505T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318505T>C , CM000674.2:g.121318505T>C	GRCh38
NC_000012.11:g.121756308T>C , CM000674.1:g.121756308T>C	GRCh37
NC_000012.10:g.120240691T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1741A>G MANE Select	ENSP00000261819.3:p.Ile581Val
ENST00000261819.7:c.1741A>G	ENSP00000261819.3:p.Ile581Val
ENST00000441917.6:c.1405A>G	ENSP00000415061.2:p.Ile469Val
ENST00000534976.5:n.2397A>G
ENST00000535482.1:c.739A>G	ENSP00000438754.1:p.Ile247Val
ENST00000535641.5:n.1952A>G
ENST00000539079.5:c.1085A>G
ENST00000541887.5:c.1702A>G	ENSP00000439875.1:p.Ile568Val
ENST00000544314.5:n.859A>G
ENST00000545218.5:n.984A>G
NM_001137559.1:c.1405A>G	NP_001131031.1:p.Ile469Val
NM_016237.4:c.1741A>G	NP_057321.2:p.Ile581Val
XM_005253900.2:c.1702A>G	XP_005253957.1:p.Ile568Val
XM_006719449.1:c.547A>G	XP_006719512.1:p.Ile183Val
NM_001330489.1:c.1702A>G	NP_001317418.1:p.Ile568Val
XM_017019423.2:c.547A>G	XP_016874912.1:p.Ile183Val
XM_017019424.2:c.547A>G	XP_016874913.1:p.Ile183Val
NM_016237.5:c.1741A>G MANE Select	NP_057321.2:p.Ile581Val
NM_001330489.2:c.1702A>G	NP_001317418.1:p.Ile568Val