Canonical Allele Identifier: CA2079394001

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882959_24882962delinsTTCC , CM000675.2:g.24882959_24882962delinsTTCC GRCh38
NC_000013.10:g.25457097_25457100delinsTTCC , CM000675.1:g.25457097_25457100delinsTTCC GRCh37
NC_000013.9:g.24355097_24355100delinsTTCC NCBI36
NG_009165.2:g.44986_44989delinsGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*215_*218delinsGGAA (CENPJ) MANE Select ENSP00000371308.4:n.*215_*218delinsGGAA
ENST00000616936.4:c.*886_*889delinsGGAA (CENPJ) ENSP00000477511.1:n.*886_*889delinsGGAA
NM_018451.4:c.*215_*218delinsGGAA (CENPJ) NP_060921.3:n.*215_*218delinsGGAA
NR_047594.1:n.4544_4547delinsGGAA (CENPJ)
NR_047595.1:n.4342_4345delinsGGAA (CENPJ)
XM_011535156.1:c.*10+3664_*10+3667delinsTTCC (RNF17) XP_011533458.1:n.*10+3664_*10+3667delinsTTCC
XM_011535156.2:c.*10+3664_*10+3667delinsTTCC (RNF17) XP_011533458.1:n.*10+3664_*10+3667delinsTTCC
NM_018451.5:c.*215_*218delinsGGAA (CENPJ) MANE Select NP_060921.3:n.*215_*218delinsGGAA
NR_047594.2:n.4516_4519delinsGGAA (CENPJ)
NR_047595.2:n.4314_4317delinsGGAA (CENPJ)