Canonical Allele Identifier: CA482430350

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756318T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318515T>A , CM000674.2:g.121318515T>A	GRCh38
NC_000012.11:g.121756318T>A , CM000674.1:g.121756318T>A	GRCh37
NC_000012.10:g.120240701T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1731A>T MANE Select	ENSP00000261819.3:p.Thr577=
ENST00000261819.7:c.1731A>T	ENSP00000261819.3:p.Thr577=
ENST00000441917.6:c.1395A>T	ENSP00000415061.2:p.Thr465=
ENST00000534976.5:n.2387A>T
ENST00000535482.1:c.729A>T	ENSP00000438754.1:p.Thr243=
ENST00000535641.5:n.1942A>T
ENST00000539079.5:c.1075A>T
ENST00000541887.5:c.1692A>T	ENSP00000439875.1:p.Thr564=
ENST00000544314.5:n.849A>T
ENST00000545218.5:n.974A>T
NM_001137559.1:c.1395A>T	NP_001131031.1:p.Thr465=
NM_016237.4:c.1731A>T	NP_057321.2:p.Thr577=
XM_005253900.2:c.1692A>T	XP_005253957.1:p.Thr564=
XM_006719449.1:c.537A>T	XP_006719512.1:p.Thr179=
NM_001330489.1:c.1692A>T	NP_001317418.1:p.Thr564=
XM_017019423.2:c.537A>T	XP_016874912.1:p.Thr179=
XM_017019424.2:c.537A>T	XP_016874913.1:p.Thr179=
NM_016237.5:c.1731A>T MANE Select	NP_057321.2:p.Thr577=
NM_001330489.2:c.1692A>T	NP_001317418.1:p.Thr564=