Canonical Allele Identifier: CA2079394078

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883104A= , CM000675.2:g.24883104A= GRCh38
NC_000013.10:g.25457242A= , CM000675.1:g.25457242A= GRCh37
NC_000013.9:g.24355242A= NCBI36
NG_009165.2:g.44844T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*73T= (CENPJ) MANE Select ENSP00000371308.4:n.*73T=
ENST00000381884.8:c.*73T= (CENPJ) ENSP00000371308.4:n.*73T=
ENST00000616936.4:c.*744T= (CENPJ) ENSP00000477511.1:n.*744T=
NM_018451.4:c.*73T= (CENPJ) NP_060921.3:n.*73T=
NR_047594.1:n.4402T= (CENPJ)
NR_047595.1:n.4200T= (CENPJ)
XM_011535156.1:c.*10+3809A= (RNF17) XP_011533458.1:n.*10+3809A=
XM_011535156.2:c.*10+3809A= (RNF17) XP_011533458.1:n.*10+3809A=
NM_018451.5:c.*73T= (CENPJ) MANE Select NP_060921.3:n.*73T=
NR_047594.2:n.4374T= (CENPJ)
NR_047595.2:n.4172T= (CENPJ)