Canonical Allele Identifier: CA2079393942
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882865T= , CM000675.2:g.24882865T= GRCh38
NC_000013.10:g.25457003T= , CM000675.1:g.25457003T= GRCh37
NC_000013.9:g.24355003T= NCBI36
NG_009165.2:g.45083A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*312A= (CENPJ) MANE Select ENSP00000371308.4:n.*312A=
ENST00000616936.4:c.*983A= (CENPJ) ENSP00000477511.1:n.*983A=
NM_018451.4:c.*312A= (CENPJ) NP_060921.3:n.*312A=
NR_047594.1:n.4641A= (CENPJ)
NR_047595.1:n.4439A= (CENPJ)
XM_011535156.1:c.*10+3570T= (RNF17) XP_011533458.1:n.*10+3570T=
XM_011535156.2:c.*10+3570T= (RNF17) XP_011533458.1:n.*10+3570T=
NM_018451.5:c.*312A= (CENPJ) MANE Select NP_060921.3:n.*312A=
NR_047594.2:n.4613A= (CENPJ)
NR_047595.2:n.4411A= (CENPJ)
Search 100 bp 5'
Search 100 bp 3'