Canonical Allele Identifier: CA2079393963

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882885T= , CM000675.2:g.24882885T= GRCh38
NC_000013.10:g.25457023T= , CM000675.1:g.25457023T= GRCh37
NC_000013.9:g.24355023T= NCBI36
NG_009165.2:g.45063A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*292A= (CENPJ) MANE Select ENSP00000371308.4:n.*292A=
ENST00000616936.4:c.*963A= (CENPJ) ENSP00000477511.1:n.*963A=
NM_018451.4:c.*292A= (CENPJ) NP_060921.3:n.*292A=
NR_047594.1:n.4621A= (CENPJ)
NR_047595.1:n.4419A= (CENPJ)
XM_011535156.1:c.*10+3590T= (RNF17) XP_011533458.1:n.*10+3590T=
XM_011535156.2:c.*10+3590T= (RNF17) XP_011533458.1:n.*10+3590T=
NM_018451.5:c.*292A= (CENPJ) MANE Select NP_060921.3:n.*292A=
NR_047594.2:n.4593A= (CENPJ)
NR_047595.2:n.4391A= (CENPJ)