Canonical Allele Identifier: CA2079393968

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882894C= , CM000675.2:g.24882894C= GRCh38
NC_000013.10:g.25457032C= , CM000675.1:g.25457032C= GRCh37
NC_000013.9:g.24355032C= NCBI36
NG_009165.2:g.45054G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*283G= (CENPJ) MANE Select ENSP00000371308.4:n.*283G=
ENST00000616936.4:c.*954G= (CENPJ) ENSP00000477511.1:n.*954G=
NM_018451.4:c.*283G= (CENPJ) NP_060921.3:n.*283G=
NR_047594.1:n.4612G= (CENPJ)
NR_047595.1:n.4410G= (CENPJ)
XM_011535156.1:c.*10+3599C= (RNF17) XP_011533458.1:n.*10+3599C=
XM_011535156.2:c.*10+3599C= (RNF17) XP_011533458.1:n.*10+3599C=
NM_018451.5:c.*283G= (CENPJ) MANE Select NP_060921.3:n.*283G=
NR_047594.2:n.4584G= (CENPJ)
NR_047595.2:n.4382G= (CENPJ)