Canonical Allele Identifier: CA386960748

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756329G>T (hg19) ; chr12:g.121318526G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318526G>T , CM000674.2:g.121318526G>T	GRCh38
NC_000012.11:g.121756329G>T , CM000674.1:g.121756329G>T	GRCh37
NC_000012.10:g.120240712G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1720C>A MANE Select	ENSP00000261819.3:p.Leu574Met
ENST00000261819.7:c.1720C>A	ENSP00000261819.3:p.Leu574Met
ENST00000441917.6:c.1384C>A	ENSP00000415061.2:p.Leu462Met
ENST00000534976.5:n.2376C>A
ENST00000535482.1:c.718C>A	ENSP00000438754.1:p.Leu240Met
ENST00000535641.5:n.1931C>A
ENST00000539079.5:c.1064C>A
ENST00000541887.5:c.1681C>A	ENSP00000439875.1:p.Leu561Met
ENST00000544314.5:n.838C>A
ENST00000545218.5:n.963C>A
NM_001137559.1:c.1384C>A	NP_001131031.1:p.Leu462Met
NM_016237.4:c.1720C>A	NP_057321.2:p.Leu574Met
XM_005253900.2:c.1681C>A	XP_005253957.1:p.Leu561Met
XM_006719449.1:c.526C>A	XP_006719512.1:p.Leu176Met
NM_001330489.1:c.1681C>A	NP_001317418.1:p.Leu561Met
XM_017019423.2:c.526C>A	XP_016874912.1:p.Leu176Met
XM_017019424.2:c.526C>A	XP_016874913.1:p.Leu176Met
NM_016237.5:c.1720C>A MANE Select	NP_057321.2:p.Leu574Met
NM_001330489.2:c.1681C>A	NP_001317418.1:p.Leu561Met