Canonical Allele Identifier: CA2079393962

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882884A= , CM000675.2:g.24882884A= GRCh38
NC_000013.10:g.25457022A= , CM000675.1:g.25457022A= GRCh37
NC_000013.9:g.24355022A= NCBI36
NG_009165.2:g.45064T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*293T= (CENPJ) MANE Select ENSP00000371308.4:n.*293T=
ENST00000616936.4:c.*964T= (CENPJ) ENSP00000477511.1:n.*964T=
NM_018451.4:c.*293T= (CENPJ) NP_060921.3:n.*293T=
NR_047594.1:n.4622T= (CENPJ)
NR_047595.1:n.4420T= (CENPJ)
XM_011535156.1:c.*10+3589A= (RNF17) XP_011533458.1:n.*10+3589A=
XM_011535156.2:c.*10+3589A= (RNF17) XP_011533458.1:n.*10+3589A=
NM_018451.5:c.*293T= (CENPJ) MANE Select NP_060921.3:n.*293T=
NR_047594.2:n.4594T= (CENPJ)
NR_047595.2:n.4392T= (CENPJ)