Canonical Allele Identifier: CA2079394096

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883124A= , CM000675.2:g.24883124A= GRCh38
NC_000013.10:g.25457262A= , CM000675.1:g.25457262A= GRCh37
NC_000013.9:g.24355262A= NCBI36
NG_009165.2:g.44824T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*53T= (CENPJ) MANE Select ENSP00000371308.4:n.*53T=
ENST00000381884.8:c.*53T= (CENPJ) ENSP00000371308.4:n.*53T=
ENST00000616936.4:c.*724T= (CENPJ) ENSP00000477511.1:n.*724T=
NM_018451.4:c.*53T= (CENPJ) NP_060921.3:n.*53T=
NR_047594.1:n.4382T= (CENPJ)
NR_047595.1:n.4180T= (CENPJ)
XM_011535156.1:c.*10+3829A= (RNF17) XP_011533458.1:n.*10+3829A=
XM_011535156.2:c.*10+3829A= (RNF17) XP_011533458.1:n.*10+3829A=
NM_018451.5:c.*53T= (CENPJ) MANE Select NP_060921.3:n.*53T=
NR_047594.2:n.4354T= (CENPJ)
NR_047595.2:n.4152T= (CENPJ)