Canonical Allele Identifier: CA386960065

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318369-G-T
• MyVariant Identifiers: chr12:g.121756172G>T (hg19) ; chr12:g.121318369G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318369G>T , CM000674.2:g.121318369G>T	GRCh38
NC_000012.11:g.121756172G>T , CM000674.1:g.121756172G>T	GRCh37
NC_000012.10:g.120240555G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1801C>A MANE Select	ENSP00000261819.3:p.Leu601Met
ENST00000261819.7:c.1801C>A	ENSP00000261819.3:p.Leu601Met
ENST00000441917.6:c.1465C>A	ENSP00000415061.2:p.Leu489Met
ENST00000534976.5:n.2533C>A
ENST00000535482.1:c.799C>A	ENSP00000438754.1:p.Leu267Met
ENST00000535641.5:n.2012C>A
ENST00000539079.5:c.1125C>A
ENST00000541887.5:c.1762C>A	ENSP00000439875.1:p.Leu588Met
ENST00000544314.5:n.919C>A
ENST00000545218.5:n.989-18C>A
NM_001137559.1:c.1465C>A	NP_001131031.1:p.Leu489Met
NM_016237.4:c.1801C>A	NP_057321.2:p.Leu601Met
XM_005253900.2:c.1762C>A	XP_005253957.1:p.Leu588Met
XM_006719449.1:c.607C>A	XP_006719512.1:p.Leu203Met
NM_001330489.1:c.1762C>A	NP_001317418.1:p.Leu588Met
XM_017019423.2:c.607C>A	XP_016874912.1:p.Leu203Met
XM_017019424.2:c.607C>A	XP_016874913.1:p.Leu203Met
NM_016237.5:c.1801C>A MANE Select	NP_057321.2:p.Leu601Met
NM_001330489.2:c.1762C>A	NP_001317418.1:p.Leu588Met