Canonical Allele Identifier: CA2622386465

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882886_24882890del , CM000675.2:g.24882886_24882890del GRCh38
NC_000013.10:g.25457024_25457028del , CM000675.1:g.25457024_25457028del GRCh37
NC_000013.9:g.24355024_24355028del NCBI36
NG_009165.2:g.45058_45062del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*287_*291del (CENPJ) MANE Select ENSP00000371308.4:n.*287_*291del
ENST00000616936.4:c.*958_*962del (CENPJ) ENSP00000477511.1:n.*958_*962del
NM_018451.4:c.*287_*291del (CENPJ) NP_060921.3:n.*287_*291del
NR_047594.1:n.4616_4620del (CENPJ)
NR_047595.1:n.4414_4418del (CENPJ)
XM_011535156.1:c.*10+3591_*10+3595del (RNF17) XP_011533458.1:n.*10+3591_*10+3595del
XM_011535156.2:c.*10+3591_*10+3595del (RNF17) XP_011533458.1:n.*10+3591_*10+3595del
NM_018451.5:c.*287_*291del (CENPJ) MANE Select NP_060921.3:n.*287_*291del
NR_047594.2:n.4588_4592del (CENPJ)
NR_047595.2:n.4386_4390del (CENPJ)