Canonical Allele Identifier: CA2079393974

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882899_24882903delinsCAATA , CM000675.2:g.24882899_24882903delinsCAATA GRCh38
NC_000013.10:g.25457037_25457041delinsCAATA , CM000675.1:g.25457037_25457041delinsCAATA GRCh37
NC_000013.9:g.24355037_24355041delinsCAATA NCBI36
NG_009165.2:g.45045_45049delinsTATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*274_*278delinsTATTG (CENPJ) MANE Select ENSP00000371308.4:n.*274_*278delinsTATTG
ENST00000616936.4:c.*945_*949delinsTATTG (CENPJ) ENSP00000477511.1:n.*945_*949delinsTATTG
NM_018451.4:c.*274_*278delinsTATTG (CENPJ) NP_060921.3:n.*274_*278delinsTATTG
NR_047594.1:n.4603_4607delinsTATTG (CENPJ)
NR_047595.1:n.4401_4405delinsTATTG (CENPJ)
XM_011535156.1:c.*10+3604_*10+3608delinsCAATA (RNF17) XP_011533458.1:n.*10+3604_*10+3608delinsCAATA
XM_011535156.2:c.*10+3604_*10+3608delinsCAATA (RNF17) XP_011533458.1:n.*10+3604_*10+3608delinsCAATA
NM_018451.5:c.*274_*278delinsTATTG (CENPJ) MANE Select NP_060921.3:n.*274_*278delinsTATTG
NR_047594.2:n.4575_4579delinsTATTG (CENPJ)
NR_047595.2:n.4373_4377delinsTATTG (CENPJ)