Canonical Allele Identifier: CA387594605

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883259C>T , CM000675.2:g.24883259C>T GRCh38
NC_000013.10:g.25457397C>T , CM000675.1:g.25457397C>T GRCh37
NC_000013.9:g.24355397C>T NCBI36
NG_009165.2:g.44689G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3935G>A (CENPJ) MANE Select ENSP00000371308.4:p.Gly1312Asp
ENST00000545981.6:c.*675G>A (CENPJ) ENSP00000441090.2:n.*675G>A
ENST00000381884.8:c.3935G>A (CENPJ) ENSP00000371308.4:p.Gly1312Asp
ENST00000545981.5:c.*676G>A (CENPJ) ENSP00000441090.2:n.*676G>A
ENST00000616936.4:c.*589G>A (CENPJ) ENSP00000477511.1:n.*589G>A
NM_018451.4:c.3935G>A (CENPJ) NP_060921.3:p.Gly1312Asp
NR_047594.1:n.4247G>A (CENPJ)
NR_047595.1:n.4045G>A (CENPJ)
XM_011535156.1:c.*10+3964C>T (RNF17) XP_011533458.1:n.*10+3964C>T
XM_011535156.2:c.*10+3964C>T (RNF17) XP_011533458.1:n.*10+3964C>T
NM_018451.5:c.3935G>A (CENPJ) MANE Select NP_060921.3:p.Gly1312Asp
NR_047594.2:n.4219G>A (CENPJ)
NR_047595.2:n.4017G>A (CENPJ)