Canonical Allele Identifier: CA2079394033

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883040G= , CM000675.2:g.24883040G= GRCh38
NC_000013.10:g.25457178G= , CM000675.1:g.25457178G= GRCh37
NC_000013.9:g.24355178G= NCBI36
NG_009165.2:g.44908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*137C= (CENPJ) MANE Select ENSP00000371308.4:n.*137C=
ENST00000381884.8:c.*137C= (CENPJ) ENSP00000371308.4:n.*137C=
ENST00000616936.4:c.*808C= (CENPJ) ENSP00000477511.1:n.*808C=
NM_018451.4:c.*137C= (CENPJ) NP_060921.3:n.*137C=
NR_047594.1:n.4466C= (CENPJ)
NR_047595.1:n.4264C= (CENPJ)
XM_011535156.1:c.*10+3745G= (RNF17) XP_011533458.1:n.*10+3745G=
XM_011535156.2:c.*10+3745G= (RNF17) XP_011533458.1:n.*10+3745G=
NM_018451.5:c.*137C= (CENPJ) MANE Select NP_060921.3:n.*137C=
NR_047594.2:n.4438C= (CENPJ)
NR_047595.2:n.4236C= (CENPJ)