Canonical Allele Identifier: CA2622386563

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883034G>T , CM000675.2:g.24883034G>T GRCh38
NC_000013.10:g.25457172G>T , CM000675.1:g.25457172G>T GRCh37
NC_000013.9:g.24355172G>T NCBI36
NG_009165.2:g.44914C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*143C>A (CENPJ) MANE Select ENSP00000371308.4:n.*143C>A
ENST00000381884.8:c.*143C>A (CENPJ) ENSP00000371308.4:n.*143C>A
ENST00000616936.4:c.*814C>A (CENPJ) ENSP00000477511.1:n.*814C>A
NM_018451.4:c.*143C>A (CENPJ) NP_060921.3:n.*143C>A
NR_047594.1:n.4472C>A (CENPJ)
NR_047595.1:n.4270C>A (CENPJ)
XM_011535156.1:c.*10+3739G>T (RNF17) XP_011533458.1:n.*10+3739G>T
XM_011535156.2:c.*10+3739G>T (RNF17) XP_011533458.1:n.*10+3739G>T
NM_018451.5:c.*143C>A (CENPJ) MANE Select NP_060921.3:n.*143C>A
NR_047594.2:n.4444C>A (CENPJ)
NR_047595.2:n.4242C>A (CENPJ)