Canonical Allele Identifier: CA387585110
Gene: CENPJ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24905645G>T , CM000675.2:g.24905645G>T GRCh38
NC_000013.10:g.25479783G>T , CM000675.1:g.25479783G>T GRCh37
NC_000013.9:g.24377783G>T NCBI36
NG_009165.2:g.22303C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.2393C>A MANE Select ENSP00000371308.4:p.Thr798Asn
ENST00000545981.6:c.2393C>A ENSP00000441090.2:p.Thr798Asn
ENST00000381884.8:c.2393C>A ENSP00000371308.4:p.Thr798Asn
ENST00000545981.5:c.2393C>A ENSP00000441090.2:p.Thr798Asn
ENST00000616936.4:c.2393C>A ENSP00000477511.1:p.Thr798Asn
NM_018451.4:c.2393C>A NP_060921.3:p.Thr798Asn
NR_047594.1:n.2588C>A
NR_047595.1:n.2588C>A
XM_011535149.1:c.2393C>A XP_011533451.1:p.Thr798Asn
XM_011535150.1:c.2393C>A XP_011533452.1:p.Thr798Asn
XM_011535151.1:c.2393C>A XP_011533453.1:p.Thr798Asn
XR_941627.1:n.2588C>A
XR_941628.1:n.2588C>A
XM_011535149.2:c.2393C>A XP_011533451.1:p.Thr798Asn
XM_011535150.2:c.2393C>A XP_011533452.1:p.Thr798Asn
XM_017020673.1:c.2393C>A XP_016876162.1:p.Thr798Asn
NM_018451.5:c.2393C>A MANE Select NP_060921.3:p.Thr798Asn
NR_047594.2:n.2560C>A
NR_047595.2:n.2560C>A