Canonical Allele Identifier: CA2079393929
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882857A= , CM000675.2:g.24882857A= GRCh38
NC_000013.10:g.25456995A= , CM000675.1:g.25456995A= GRCh37
NC_000013.9:g.24354995A= NCBI36
NG_009165.2:g.45091T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*320T= (CENPJ) MANE Select ENSP00000371308.4:n.*320T=
ENST00000616936.4:c.*991T= (CENPJ) ENSP00000477511.1:n.*991T=
NM_018451.4:c.*320T= (CENPJ) NP_060921.3:n.*320T=
NR_047594.1:n.4649T= (CENPJ)
NR_047595.1:n.4447T= (CENPJ)
XM_011535156.1:c.*10+3562A= (RNF17) XP_011533458.1:n.*10+3562A=
XM_011535156.2:c.*10+3562A= (RNF17) XP_011533458.1:n.*10+3562A=
NM_018451.5:c.*320T= (CENPJ) MANE Select NP_060921.3:n.*320T=
NR_047594.2:n.4621T= (CENPJ)
NR_047595.2:n.4419T= (CENPJ)
Search 100 bp 5'
Search 100 bp 3'