Canonical Allele Identifier: CA2079394110

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883144_24883150delinsAGTTACT , CM000675.2:g.24883144_24883150delinsAGTTACT GRCh38
NC_000013.10:g.25457282_25457288delinsAGTTACT , CM000675.1:g.25457282_25457288delinsAGTTACT GRCh37
NC_000013.9:g.24355282_24355288delinsAGTTACT NCBI36
NG_009165.2:g.44798_44804delinsAGTAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*27_*33delinsAGTAACT (CENPJ) MANE Select ENSP00000371308.4:n.*27_*33delinsAGTAACT
ENST00000381884.8:c.*27_*33delinsAGTAACT (CENPJ) ENSP00000371308.4:n.*27_*33delinsAGTAACT
ENST00000616936.4:c.*698_*704delinsAGTAACT (CENPJ) ENSP00000477511.1:n.*698_*704delinsAGTAACT
NM_018451.4:c.*27_*33delinsAGTAACT (CENPJ) NP_060921.3:n.*27_*33delinsAGTAACT
NR_047594.1:n.4356_4362delinsAGTAACT (CENPJ)
NR_047595.1:n.4154_4160delinsAGTAACT (CENPJ)
XM_011535156.1:c.*10+3849_*10+3855delinsAGTTACT (RNF17) XP_011533458.1:n.*10+3849_*10+3855delinsAGTTACT
XM_011535156.2:c.*10+3849_*10+3855delinsAGTTACT (RNF17) XP_011533458.1:n.*10+3849_*10+3855delinsAGTTACT
NM_018451.5:c.*27_*33delinsAGTAACT (CENPJ) MANE Select NP_060921.3:n.*27_*33delinsAGTAACT
NR_047594.2:n.4328_4334delinsAGTAACT (CENPJ)
NR_047595.2:n.4126_4132delinsAGTAACT (CENPJ)