Canonical Allele Identifier: CA2079393928

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882854T= , CM000675.2:g.24882854T= GRCh38
NC_000013.10:g.25456992T= , CM000675.1:g.25456992T= GRCh37
NC_000013.9:g.24354992T= NCBI36
NG_009165.2:g.45094A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*323A= (CENPJ) MANE Select ENSP00000371308.4:n.*323A=
ENST00000616936.4:c.*994A= (CENPJ) ENSP00000477511.1:n.*994A=
NM_018451.4:c.*323A= (CENPJ) NP_060921.3:n.*323A=
NR_047594.1:n.4652A= (CENPJ)
NR_047595.1:n.4450A= (CENPJ)
XM_011535156.1:c.*10+3559T= (RNF17) XP_011533458.1:n.*10+3559T=
XM_011535156.2:c.*10+3559T= (RNF17) XP_011533458.1:n.*10+3559T=
NM_018451.5:c.*323A= (CENPJ) MANE Select NP_060921.3:n.*323A=
NR_047594.2:n.4624A= (CENPJ)
NR_047595.2:n.4422A= (CENPJ)