Canonical Allele Identifier: CA2798539587

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882850G>C , CM000675.2:g.24882850G>C GRCh38
NC_000013.10:g.25456988G>C , CM000675.1:g.25456988G>C GRCh37
NC_000013.9:g.24354988G>C NCBI36
NG_009165.2:g.45098C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*327C>G (CENPJ) MANE Select ENSP00000371308.4:n.*327C>G
ENST00000616936.4:c.*998C>G (CENPJ) ENSP00000477511.1:n.*998C>G
NM_018451.4:c.*327C>G (CENPJ) NP_060921.3:n.*327C>G
NR_047594.1:n.4656C>G (CENPJ)
NR_047595.1:n.4454C>G (CENPJ)
XM_011535156.1:c.*10+3555G>C (RNF17) XP_011533458.1:n.*10+3555G>C
XM_011535156.2:c.*10+3555G>C (RNF17) XP_011533458.1:n.*10+3555G>C
NM_018451.5:c.*327C>G (CENPJ) MANE Select NP_060921.3:n.*327C>G
NR_047594.2:n.4628C>G (CENPJ)
NR_047595.2:n.4426C>G (CENPJ)