Canonical Allele Identifier: CA2079394025

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883006A= , CM000675.2:g.24883006A= GRCh38
NC_000013.10:g.25457144A= , CM000675.1:g.25457144A= GRCh37
NC_000013.9:g.24355144A= NCBI36
NG_009165.2:g.44942T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*171T= (CENPJ) MANE Select ENSP00000371308.4:n.*171T=
ENST00000616936.4:c.*842T= (CENPJ) ENSP00000477511.1:n.*842T=
NM_018451.4:c.*171T= (CENPJ) NP_060921.3:n.*171T=
NR_047594.1:n.4500T= (CENPJ)
NR_047595.1:n.4298T= (CENPJ)
XM_011535156.1:c.*10+3711A= (RNF17) XP_011533458.1:n.*10+3711A=
XM_011535156.2:c.*10+3711A= (RNF17) XP_011533458.1:n.*10+3711A=
NM_018451.5:c.*171T= (CENPJ) MANE Select NP_060921.3:n.*171T=
NR_047594.2:n.4472T= (CENPJ)
NR_047595.2:n.4270T= (CENPJ)