Canonical Allele Identifier: CA387594598

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883256T>A , CM000675.2:g.24883256T>A GRCh38
NC_000013.10:g.25457394T>A , CM000675.1:g.25457394T>A GRCh37
NC_000013.9:g.24355394T>A NCBI36
NG_009165.2:g.44692A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3938A>T (CENPJ) MANE Select ENSP00000371308.4:p.His1313Leu
ENST00000545981.6:c.*678A>T (CENPJ) ENSP00000441090.2:n.*678A>T
ENST00000381884.8:c.3938A>T (CENPJ) ENSP00000371308.4:p.His1313Leu
ENST00000545981.5:c.*679A>T (CENPJ) ENSP00000441090.2:n.*679A>T
ENST00000616936.4:c.*592A>T (CENPJ) ENSP00000477511.1:n.*592A>T
NM_018451.4:c.3938A>T (CENPJ) NP_060921.3:p.His1313Leu
NR_047594.1:n.4250A>T (CENPJ)
NR_047595.1:n.4048A>T (CENPJ)
XM_011535156.1:c.*10+3961T>A (RNF17) XP_011533458.1:n.*10+3961T>A
XM_011535156.2:c.*10+3961T>A (RNF17) XP_011533458.1:n.*10+3961T>A
NM_018451.5:c.3938A>T (CENPJ) MANE Select NP_060921.3:p.His1313Leu
NR_047594.2:n.4222A>T (CENPJ)
NR_047595.2:n.4020A>T (CENPJ)