Canonical Allele Identifier: CA6919595
Gene: CENPJ HGNC NCBI

Linked Data

dbSNP Id: rs749518656

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24905582dup , CM000675.2:g.24905582dup GRCh38
NC_000013.10:g.25479720dup , CM000675.1:g.25479720dup GRCh37
NC_000013.9:g.24377720dup NCBI36
NG_009165.2:g.22366dup

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.2456dup MANE Select ENSP00000371308.4:p.Tyr819Ter
ENST00000545981.6:c.2456dup ENSP00000441090.2:p.Tyr819Ter
ENST00000381884.8:c.2456dup ENSP00000371308.4:p.Tyr819Ter
ENST00000545981.5:c.2456dup ENSP00000441090.2:p.Tyr819Ter
ENST00000616936.4:c.2456dup ENSP00000477511.1:p.Tyr819Ter
NM_018451.4:c.2456dup NP_060921.3:p.Tyr819Ter
NR_047594.1:n.2651dup
NR_047595.1:n.2651dup
XM_011535149.1:c.2456dup XP_011533451.1:p.Tyr819Ter
XM_011535150.1:c.2456dup XP_011533452.1:p.Tyr819Ter
XM_011535151.1:c.2456dup XP_011533453.1:p.Tyr819Ter
XR_941627.1:n.2651dup
XR_941628.1:n.2651dup
XM_011535149.2:c.2456dup XP_011533451.1:p.Tyr819Ter
XM_011535150.2:c.2456dup XP_011533452.1:p.Tyr819Ter
XM_017020673.1:c.2456dup XP_016876162.1:p.Tyr819Ter
NM_018451.5:c.2456dup MANE Select NP_060921.3:p.Tyr819Ter
NR_047594.2:n.2623dup
NR_047595.2:n.2623dup