Canonical Allele Identifier: CA2622386495

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882912del , CM000675.2:g.24882912del GRCh38
NC_000013.10:g.25457050del , CM000675.1:g.25457050del GRCh37
NC_000013.9:g.24355050del NCBI36
NG_009165.2:g.45038del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*267del (CENPJ) MANE Select ENSP00000371308.4:n.*267del
ENST00000616936.4:c.*938del (CENPJ) ENSP00000477511.1:n.*938del
NM_018451.4:c.*267del (CENPJ) NP_060921.3:n.*267del
NR_047594.1:n.4596del (CENPJ)
NR_047595.1:n.4394del (CENPJ)
XM_011535156.1:c.*10+3617del (RNF17) XP_011533458.1:n.*10+3617del
XM_011535156.2:c.*10+3617del (RNF17) XP_011533458.1:n.*10+3617del
NM_018451.5:c.*267del (CENPJ) MANE Select NP_060921.3:n.*267del
NR_047594.2:n.4568del (CENPJ)
NR_047595.2:n.4366del (CENPJ)