Canonical Allele Identifier: CA386961307
Gene: ANAPC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121318576A>T , CM000674.2:g.121318576A>T GRCh38
NC_000012.11:g.121756379A>T , CM000674.1:g.121756379A>T GRCh37
NC_000012.10:g.120240762A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261819.8:c.1670T>A MANE Select ENSP00000261819.3:p.Met557Lys
ENST00000261819.7:c.1670T>A ENSP00000261819.3:p.Met557Lys
ENST00000366333.3:n.882T>A
ENST00000441917.6:c.1334T>A ENSP00000415061.2:p.Met445Lys
ENST00000534976.5:n.2326T>A
ENST00000535482.1:c.668T>A ENSP00000438754.1:p.Met223Lys
ENST00000535641.5:n.1881T>A
ENST00000539079.5:c.1014T>A
ENST00000541887.5:c.1631T>A ENSP00000439875.1:p.Met544Lys
ENST00000544314.5:n.788T>A
ENST00000545218.5:n.913T>A
NM_001137559.1:c.1334T>A NP_001131031.1:p.Met445Lys
NM_016237.4:c.1670T>A NP_057321.2:p.Met557Lys
XM_005253900.2:c.1631T>A XP_005253957.1:p.Met544Lys
XM_006719449.1:c.476T>A XP_006719512.1:p.Met159Lys
NM_001330489.1:c.1631T>A NP_001317418.1:p.Met544Lys
XM_017019423.2:c.476T>A XP_016874912.1:p.Met159Lys
XM_017019424.2:c.476T>A XP_016874913.1:p.Met159Lys
NM_016237.5:c.1670T>A MANE Select NP_057321.2:p.Met557Lys
NM_001330489.2:c.1631T>A NP_001317418.1:p.Met544Lys