Canonical Allele Identifier: CA2798539586

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882847del , CM000675.2:g.24882847del GRCh38
NC_000013.10:g.25456985del , CM000675.1:g.25456985del GRCh37
NC_000013.9:g.24354985del NCBI36
NG_009165.2:g.45101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*330del (CENPJ) MANE Select ENSP00000371308.4:n.*330del
ENST00000616936.4:c.*1001del (CENPJ) ENSP00000477511.1:n.*1001del
NM_018451.4:c.*330del (CENPJ) NP_060921.3:n.*330del
NR_047594.1:n.4659del (CENPJ)
NR_047595.1:n.4457del (CENPJ)
XM_011535156.1:c.*10+3552del (RNF17) XP_011533458.1:n.*10+3552del
XM_011535156.2:c.*10+3552del (RNF17) XP_011533458.1:n.*10+3552del
NM_018451.5:c.*330del (CENPJ) MANE Select NP_060921.3:n.*330del
NR_047594.2:n.4631del (CENPJ)
NR_047595.2:n.4429del (CENPJ)