Canonical Allele Identifier: CA387594617

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883265G>C , CM000675.2:g.24883265G>C GRCh38
NC_000013.10:g.25457403G>C , CM000675.1:g.25457403G>C GRCh37
NC_000013.9:g.24355403G>C NCBI36
NG_009165.2:g.44683C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3929C>G (CENPJ) MANE Select ENSP00000371308.4:p.Ala1310Gly
ENST00000545981.6:c.*669C>G (CENPJ) ENSP00000441090.2:n.*669C>G
ENST00000381884.8:c.3929C>G (CENPJ) ENSP00000371308.4:p.Ala1310Gly
ENST00000545981.5:c.*670C>G (CENPJ) ENSP00000441090.2:n.*670C>G
ENST00000616936.4:c.*583C>G (CENPJ) ENSP00000477511.1:n.*583C>G
NM_018451.4:c.3929C>G (CENPJ) NP_060921.3:p.Ala1310Gly
NR_047594.1:n.4241C>G (CENPJ)
NR_047595.1:n.4039C>G (CENPJ)
XM_011535156.1:c.*10+3970G>C (RNF17) XP_011533458.1:n.*10+3970G>C
XM_011535156.2:c.*10+3970G>C (RNF17) XP_011533458.1:n.*10+3970G>C
NM_018451.5:c.3929C>G (CENPJ) MANE Select NP_060921.3:p.Ala1310Gly
NR_047594.2:n.4213C>G (CENPJ)
NR_047595.2:n.4011C>G (CENPJ)