Canonical Allele Identifier: CA2079393953

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882874G= , CM000675.2:g.24882874G= GRCh38
NC_000013.10:g.25457012G= , CM000675.1:g.25457012G= GRCh37
NC_000013.9:g.24355012G= NCBI36
NG_009165.2:g.45074C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*303C= (CENPJ) MANE Select ENSP00000371308.4:n.*303C=
ENST00000616936.4:c.*974C= (CENPJ) ENSP00000477511.1:n.*974C=
NM_018451.4:c.*303C= (CENPJ) NP_060921.3:n.*303C=
NR_047594.1:n.4632C= (CENPJ)
NR_047595.1:n.4430C= (CENPJ)
XM_011535156.1:c.*10+3579G= (RNF17) XP_011533458.1:n.*10+3579G=
XM_011535156.2:c.*10+3579G= (RNF17) XP_011533458.1:n.*10+3579G=
NM_018451.5:c.*303C= (CENPJ) MANE Select NP_060921.3:n.*303C=
NR_047594.2:n.4604C= (CENPJ)
NR_047595.2:n.4402C= (CENPJ)