Canonical Allele Identifier: CA2079393938
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882864G= , CM000675.2:g.24882864G= GRCh38
NC_000013.10:g.25457002G= , CM000675.1:g.25457002G= GRCh37
NC_000013.9:g.24355002G= NCBI36
NG_009165.2:g.45084C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*313C= (CENPJ) MANE Select ENSP00000371308.4:n.*313C=
ENST00000616936.4:c.*984C= (CENPJ) ENSP00000477511.1:n.*984C=
NM_018451.4:c.*313C= (CENPJ) NP_060921.3:n.*313C=
NR_047594.1:n.4642C= (CENPJ)
NR_047595.1:n.4440C= (CENPJ)
XM_011535156.1:c.*10+3569G= (RNF17) XP_011533458.1:n.*10+3569G=
XM_011535156.2:c.*10+3569G= (RNF17) XP_011533458.1:n.*10+3569G=
NM_018451.5:c.*313C= (CENPJ) MANE Select NP_060921.3:n.*313C=
NR_047594.2:n.4614C= (CENPJ)
NR_047595.2:n.4412C= (CENPJ)
Search 100 bp 5'
Search 100 bp 3'