Canonical Allele Identifier: CA386959682

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756135T>A (hg19) ; chr12:g.121318332T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318332T>A , CM000674.2:g.121318332T>A	GRCh38
NC_000012.11:g.121756135T>A , CM000674.1:g.121756135T>A	GRCh37
NC_000012.10:g.120240518T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1838A>T MANE Select	ENSP00000261819.3:p.Glu613Val
ENST00000261819.7:c.1838A>T	ENSP00000261819.3:p.Glu613Val
ENST00000441917.6:c.1502A>T	ENSP00000415061.2:p.Glu501Val
ENST00000534976.5:n.2570A>T
ENST00000535482.1:c.836A>T	ENSP00000438754.1:p.Glu279Val
ENST00000535641.5:n.2049A>T
ENST00000539079.5:c.1162A>T
ENST00000541887.5:c.1799A>T	ENSP00000439875.1:p.Glu600Val
ENST00000544314.5:n.956A>T
ENST00000545218.5:n.1008A>T
NM_001137559.1:c.1502A>T	NP_001131031.1:p.Glu501Val
NM_016237.4:c.1838A>T	NP_057321.2:p.Glu613Val
XM_005253900.2:c.1799A>T	XP_005253957.1:p.Glu600Val
XM_006719449.1:c.644A>T	XP_006719512.1:p.Glu215Val
NM_001330489.1:c.1799A>T	NP_001317418.1:p.Glu600Val
XM_017019423.2:c.644A>T	XP_016874912.1:p.Glu215Val
XM_017019424.2:c.644A>T	XP_016874913.1:p.Glu215Val
NM_016237.5:c.1838A>T MANE Select	NP_057321.2:p.Glu613Val
NM_001330489.2:c.1799A>T	NP_001317418.1:p.Glu600Val