Canonical Allele Identifier: CA2079394091

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883119_24883120delinsTG , CM000675.2:g.24883119_24883120delinsTG GRCh38
NC_000013.10:g.25457257_25457258delinsTG , CM000675.1:g.25457257_25457258delinsTG GRCh37
NC_000013.9:g.24355257_24355258delinsTG NCBI36
NG_009165.2:g.44828_44829delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*57_*58delinsCA (CENPJ) MANE Select ENSP00000371308.4:n.*57_*58delinsCA
ENST00000381884.8:c.*57_*58delinsCA (CENPJ) ENSP00000371308.4:n.*57_*58delinsCA
ENST00000616936.4:c.*728_*729delinsCA (CENPJ) ENSP00000477511.1:n.*728_*729delinsCA
NM_018451.4:c.*57_*58delinsCA (CENPJ) NP_060921.3:n.*57_*58delinsCA
NR_047594.1:n.4386_4387delinsCA (CENPJ)
NR_047595.1:n.4184_4185delinsCA (CENPJ)
XM_011535156.1:c.*10+3824_*10+3825delinsTG (RNF17) XP_011533458.1:n.*10+3824_*10+3825delinsTG
XM_011535156.2:c.*10+3824_*10+3825delinsTG (RNF17) XP_011533458.1:n.*10+3824_*10+3825delinsTG
NM_018451.5:c.*57_*58delinsCA (CENPJ) MANE Select NP_060921.3:n.*57_*58delinsCA
NR_047594.2:n.4358_4359delinsCA (CENPJ)
NR_047595.2:n.4156_4157delinsCA (CENPJ)