Canonical Allele Identifier: CA386960791
Gene: ANAPC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121318530C>A , CM000674.2:g.121318530C>A GRCh38
NC_000012.11:g.121756333C>A , CM000674.1:g.121756333C>A GRCh37
NC_000012.10:g.120240716C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261819.8:c.1716G>T MANE Select ENSP00000261819.3:p.Gln572His
ENST00000261819.7:c.1716G>T ENSP00000261819.3:p.Gln572His
ENST00000441917.6:c.1380G>T ENSP00000415061.2:p.Gln460His
ENST00000534976.5:n.2372G>T
ENST00000535482.1:c.714G>T ENSP00000438754.1:p.Gln238His
ENST00000535641.5:n.1927G>T
ENST00000539079.5:c.1060G>T
ENST00000541887.5:c.1677G>T ENSP00000439875.1:p.Gln559His
ENST00000544314.5:n.834G>T
ENST00000545218.5:n.959G>T
NM_001137559.1:c.1380G>T NP_001131031.1:p.Gln460His
NM_016237.4:c.1716G>T NP_057321.2:p.Gln572His
XM_005253900.2:c.1677G>T XP_005253957.1:p.Gln559His
XM_006719449.1:c.522G>T XP_006719512.1:p.Gln174His
NM_001330489.1:c.1677G>T NP_001317418.1:p.Gln559His
XM_017019423.2:c.522G>T XP_016874912.1:p.Gln174His
XM_017019424.2:c.522G>T XP_016874913.1:p.Gln174His
NM_016237.5:c.1716G>T MANE Select NP_057321.2:p.Gln572His
NM_001330489.2:c.1677G>T NP_001317418.1:p.Gln559His