Canonical Allele Identifier: CA2079393946

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882868T= , CM000675.2:g.24882868T= GRCh38
NC_000013.10:g.25457006T= , CM000675.1:g.25457006T= GRCh37
NC_000013.9:g.24355006T= NCBI36
NG_009165.2:g.45080A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*309A= (CENPJ) MANE Select ENSP00000371308.4:n.*309A=
ENST00000616936.4:c.*980A= (CENPJ) ENSP00000477511.1:n.*980A=
NM_018451.4:c.*309A= (CENPJ) NP_060921.3:n.*309A=
NR_047594.1:n.4638A= (CENPJ)
NR_047595.1:n.4436A= (CENPJ)
XM_011535156.1:c.*10+3573T= (RNF17) XP_011533458.1:n.*10+3573T=
XM_011535156.2:c.*10+3573T= (RNF17) XP_011533458.1:n.*10+3573T=
NM_018451.5:c.*309A= (CENPJ) MANE Select NP_060921.3:n.*309A=
NR_047594.2:n.4610A= (CENPJ)
NR_047595.2:n.4408A= (CENPJ)