Canonical Allele Identifier: CA386959404
Gene: ANAPC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121318304T>A , CM000674.2:g.121318304T>A GRCh38
NC_000012.11:g.121756107T>A , CM000674.1:g.121756107T>A GRCh37
NC_000012.10:g.120240490T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261819.8:c.1866A>T MANE Select ENSP00000261819.3:p.Glu622Asp
ENST00000261819.7:c.1866A>T ENSP00000261819.3:p.Glu622Asp
ENST00000441917.6:c.1530A>T ENSP00000415061.2:p.Glu510Asp
ENST00000534976.5:n.2598A>T
ENST00000535482.1:c.864A>T ENSP00000438754.1:p.Glu288Asp
ENST00000535641.5:n.2077A>T
ENST00000539079.5:c.1190A>T
ENST00000541887.5:c.1827A>T ENSP00000439875.1:p.Glu609Asp
ENST00000544314.5:n.984A>T
ENST00000545218.5:n.1036A>T
NM_001137559.1:c.1530A>T NP_001131031.1:p.Glu510Asp
NM_016237.4:c.1866A>T NP_057321.2:p.Glu622Asp
XM_005253900.2:c.1827A>T XP_005253957.1:p.Glu609Asp
XM_006719449.1:c.672A>T XP_006719512.1:p.Glu224Asp
NM_001330489.1:c.1827A>T NP_001317418.1:p.Glu609Asp
XM_017019423.2:c.672A>T XP_016874912.1:p.Glu224Asp
XM_017019424.2:c.672A>T XP_016874913.1:p.Glu224Asp
NM_016237.5:c.1866A>T MANE Select NP_057321.2:p.Glu622Asp
NM_001330489.2:c.1827A>T NP_001317418.1:p.Glu609Asp