Canonical Allele Identifier: CA2079382440
Gene: CENPJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24905626C= , CM000675.2:g.24905626C= GRCh38
NC_000013.10:g.25479764C= , CM000675.1:g.25479764C= GRCh37
NC_000013.9:g.24377764C= NCBI36
NG_009165.2:g.22322G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.2412G= MANE Select ENSP00000371308.4:p.Glu804=
ENST00000545981.6:c.2412G= ENSP00000441090.2:p.Glu804=
ENST00000381884.8:c.2412G= ENSP00000371308.4:p.Glu804=
ENST00000545981.5:c.2412G= ENSP00000441090.2:p.Glu804=
ENST00000616936.4:c.2412G= ENSP00000477511.1:p.Glu804=
NM_018451.4:c.2412G= NP_060921.3:p.Glu804=
NR_047594.1:n.2607G=
NR_047595.1:n.2607G=
XM_011535149.1:c.2412G= XP_011533451.1:p.Glu804=
XM_011535150.1:c.2412G= XP_011533452.1:p.Glu804=
XM_011535151.1:c.2412G= XP_011533453.1:p.Glu804=
XR_941627.1:n.2607G=
XR_941628.1:n.2607G=
XM_011535149.2:c.2412G= XP_011533451.1:p.Glu804=
XM_011535150.2:c.2412G= XP_011533452.1:p.Glu804=
XM_017020673.1:c.2412G= XP_016876162.1:p.Glu804=
NM_018451.5:c.2412G= MANE Select NP_060921.3:p.Glu804=
NR_047594.2:n.2579G=
NR_047595.2:n.2579G=