Canonical Allele Identifier: CA2079394004

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882966G= , CM000675.2:g.24882966G= GRCh38
NC_000013.10:g.25457104G= , CM000675.1:g.25457104G= GRCh37
NC_000013.9:g.24355104G= NCBI36
NG_009165.2:g.44982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*211C= (CENPJ) MANE Select ENSP00000371308.4:n.*211C=
ENST00000616936.4:c.*882C= (CENPJ) ENSP00000477511.1:n.*882C=
NM_018451.4:c.*211C= (CENPJ) NP_060921.3:n.*211C=
NR_047594.1:n.4540C= (CENPJ)
NR_047595.1:n.4338C= (CENPJ)
XM_011535156.1:c.*10+3671G= (RNF17) XP_011533458.1:n.*10+3671G=
XM_011535156.2:c.*10+3671G= (RNF17) XP_011533458.1:n.*10+3671G=
NM_018451.5:c.*211C= (CENPJ) MANE Select NP_060921.3:n.*211C=
NR_047594.2:n.4512C= (CENPJ)
NR_047595.2:n.4310C= (CENPJ)