Canonical Allele Identifier: CA387576547

Linked Data

dbSNP Id: rs121434311

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24884083T>C , CM000675.2:g.24884083T>C GRCh38
NC_000013.10:g.25458221T>C , CM000675.1:g.25458221T>C GRCh37
NC_000013.9:g.24356221T>C NCBI36
NG_009165.2:g.43865A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3704A>G (CENPJ) MANE Select ENSP00000371308.4:p.Glu1235Gly
ENST00000545981.6:c.*444A>G (CENPJ) ENSP00000441090.2:n.*444A>G
ENST00000381884.8:c.3704A>G (CENPJ) ENSP00000371308.4:p.Glu1235Gly
ENST00000545981.5:c.*445A>G (CENPJ) ENSP00000441090.2:n.*445A>G
ENST00000616936.4:c.*358A>G (CENPJ) ENSP00000477511.1:n.*358A>G
NM_018451.4:c.3704A>G (CENPJ) NP_060921.3:p.Glu1235Gly
NR_047594.1:n.4016A>G (CENPJ)
NR_047595.1:n.3814A>G (CENPJ)
XM_011535156.1:c.*11-4031T>C (RNF17) XP_011533458.1:n.*11-4031T>C
XM_011535156.2:c.*11-4031T>C (RNF17) XP_011533458.1:n.*11-4031T>C
NM_018451.5:c.3704A>G (CENPJ) MANE Select NP_060921.3:p.Glu1235Gly
NR_047594.2:n.3988A>G (CENPJ)
NR_047595.2:n.3786A>G (CENPJ)