Canonical Allele Identifier: CA2079393950

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882872_24882873delinsTG , CM000675.2:g.24882872_24882873delinsTG GRCh38
NC_000013.10:g.25457010_25457011delinsTG , CM000675.1:g.25457010_25457011delinsTG GRCh37
NC_000013.9:g.24355010_24355011delinsTG NCBI36
NG_009165.2:g.45075_45076delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*304_*305delinsCA (CENPJ) MANE Select ENSP00000371308.4:n.*304_*305delinsCA
ENST00000616936.4:c.*975_*976delinsCA (CENPJ) ENSP00000477511.1:n.*975_*976delinsCA
NM_018451.4:c.*304_*305delinsCA (CENPJ) NP_060921.3:n.*304_*305delinsCA
NR_047594.1:n.4633_4634delinsCA (CENPJ)
NR_047595.1:n.4431_4432delinsCA (CENPJ)
XM_011535156.1:c.*10+3577_*10+3578delinsTG (RNF17) XP_011533458.1:n.*10+3577_*10+3578delinsTG
XM_011535156.2:c.*10+3577_*10+3578delinsTG (RNF17) XP_011533458.1:n.*10+3577_*10+3578delinsTG
NM_018451.5:c.*304_*305delinsCA (CENPJ) MANE Select NP_060921.3:n.*304_*305delinsCA
NR_047594.2:n.4605_4606delinsCA (CENPJ)
NR_047595.2:n.4403_4404delinsCA (CENPJ)