Canonical Allele Identifier: CA2079394056

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883080_24883082delinsCCA , CM000675.2:g.24883080_24883082delinsCCA GRCh38
NC_000013.10:g.25457218_25457220delinsCCA , CM000675.1:g.25457218_25457220delinsCCA GRCh37
NC_000013.9:g.24355218_24355220delinsCCA NCBI36
NG_009165.2:g.44866_44868delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*95_*97delinsTGG (CENPJ) MANE Select ENSP00000371308.4:n.*95_*97delinsTGG
ENST00000381884.8:c.*95_*97delinsTGG (CENPJ) ENSP00000371308.4:n.*95_*97delinsTGG
ENST00000616936.4:c.*766_*768delinsTGG (CENPJ) ENSP00000477511.1:n.*766_*768delinsTGG
NM_018451.4:c.*95_*97delinsTGG (CENPJ) NP_060921.3:n.*95_*97delinsTGG
NR_047594.1:n.4424_4426delinsTGG (CENPJ)
NR_047595.1:n.4222_4224delinsTGG (CENPJ)
XM_011535156.1:c.*10+3785_*10+3787delinsCCA (RNF17) XP_011533458.1:n.*10+3785_*10+3787delinsCCA
XM_011535156.2:c.*10+3785_*10+3787delinsCCA (RNF17) XP_011533458.1:n.*10+3785_*10+3787delinsCCA
NM_018451.5:c.*95_*97delinsTGG (CENPJ) MANE Select NP_060921.3:n.*95_*97delinsTGG
NR_047594.2:n.4396_4398delinsTGG (CENPJ)
NR_047595.2:n.4194_4196delinsTGG (CENPJ)