Canonical Allele Identifier: CA2622386510

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882928del , CM000675.2:g.24882928del GRCh38
NC_000013.10:g.25457066del , CM000675.1:g.25457066del GRCh37
NC_000013.9:g.24355066del NCBI36
NG_009165.2:g.45021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*250del (CENPJ) MANE Select ENSP00000371308.4:n.*250del
ENST00000616936.4:c.*921del (CENPJ) ENSP00000477511.1:n.*921del
NM_018451.4:c.*250del (CENPJ) NP_060921.3:n.*250del
NR_047594.1:n.4579del (CENPJ)
NR_047595.1:n.4377del (CENPJ)
XM_011535156.1:c.*10+3633del (RNF17) XP_011533458.1:n.*10+3633del
XM_011535156.2:c.*10+3633del (RNF17) XP_011533458.1:n.*10+3633del
NM_018451.5:c.*250del (CENPJ) MANE Select NP_060921.3:n.*250del
NR_047594.2:n.4551del (CENPJ)
NR_047595.2:n.4349del (CENPJ)