Canonical Allele Identifier: CA2798539593

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882937A>T , CM000675.2:g.24882937A>T GRCh38
NC_000013.10:g.25457075A>T , CM000675.1:g.25457075A>T GRCh37
NC_000013.9:g.24355075A>T NCBI36
NG_009165.2:g.45011T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*240T>A (CENPJ) MANE Select ENSP00000371308.4:n.*240T>A
ENST00000616936.4:c.*911T>A (CENPJ) ENSP00000477511.1:n.*911T>A
NM_018451.4:c.*240T>A (CENPJ) NP_060921.3:n.*240T>A
NR_047594.1:n.4569T>A (CENPJ)
NR_047595.1:n.4367T>A (CENPJ)
XM_011535156.1:c.*10+3642A>T (RNF17) XP_011533458.1:n.*10+3642A>T
XM_011535156.2:c.*10+3642A>T (RNF17) XP_011533458.1:n.*10+3642A>T
NM_018451.5:c.*240T>A (CENPJ) MANE Select NP_060921.3:n.*240T>A
NR_047594.2:n.4541T>A (CENPJ)
NR_047595.2:n.4339T>A (CENPJ)