Canonical Allele Identifier: CA386960211

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756187A>T (hg19) ; chr12:g.121318384A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318384A>T , CM000674.2:g.121318384A>T	GRCh38
NC_000012.11:g.121756187A>T , CM000674.1:g.121756187A>T	GRCh37
NC_000012.10:g.120240570A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1786T>A MANE Select	ENSP00000261819.3:p.Ser596Thr
ENST00000261819.7:c.1786T>A	ENSP00000261819.3:p.Ser596Thr
ENST00000441917.6:c.1450T>A	ENSP00000415061.2:p.Ser484Thr
ENST00000534976.5:n.2518T>A
ENST00000535482.1:c.784T>A	ENSP00000438754.1:p.Ser262Thr
ENST00000535641.5:n.1997T>A
ENST00000539079.5:c.1110T>A
ENST00000541887.5:c.1747T>A	ENSP00000439875.1:p.Ser583Thr
ENST00000544314.5:n.904T>A
ENST00000545218.5:n.989-33T>A
NM_001137559.1:c.1450T>A	NP_001131031.1:p.Ser484Thr
NM_016237.4:c.1786T>A	NP_057321.2:p.Ser596Thr
XM_005253900.2:c.1747T>A	XP_005253957.1:p.Ser583Thr
XM_006719449.1:c.592T>A	XP_006719512.1:p.Ser198Thr
NM_001330489.1:c.1747T>A	NP_001317418.1:p.Ser583Thr
XM_017019423.2:c.592T>A	XP_016874912.1:p.Ser198Thr
XM_017019424.2:c.592T>A	XP_016874913.1:p.Ser198Thr
NM_016237.5:c.1786T>A MANE Select	NP_057321.2:p.Ser596Thr
NM_001330489.2:c.1747T>A	NP_001317418.1:p.Ser583Thr