Canonical Allele Identifier: CA2622386686
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

gnomAD v4: 13-24883261-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883264dup , CM000675.2:g.24883264dup GRCh38
NC_000013.10:g.25457402dup , CM000675.1:g.25457402dup GRCh37
NC_000013.9:g.24355402dup NCBI36
NG_009165.2:g.44686dup

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3932dup (CENPJ) MANE Select ENSP00000371308.4:p.Asn1311LysfsTer16
ENST00000545981.6:c.*672dup (CENPJ) ENSP00000441090.2:n.*672dup
ENST00000381884.8:c.3932dup (CENPJ) ENSP00000371308.4:p.Asn1311LysfsTer16
ENST00000545981.5:c.*673dup (CENPJ) ENSP00000441090.2:n.*673dup
ENST00000616936.4:c.*586dup (CENPJ) ENSP00000477511.1:n.*586dup
NM_018451.4:c.3932dup (CENPJ) NP_060921.3:p.Asn1311LysfsTer16
NR_047594.1:n.4244dup (CENPJ)
NR_047595.1:n.4042dup (CENPJ)
XM_011535156.1:c.*10+3969dup (RNF17) XP_011533458.1:n.*10+3969dup
XM_011535156.2:c.*10+3969dup (RNF17) XP_011533458.1:n.*10+3969dup
NM_018451.5:c.3932dup (CENPJ) MANE Select NP_060921.3:p.Asn1311LysfsTer16
NR_047594.2:n.4216dup (CENPJ)
NR_047595.2:n.4014dup (CENPJ)
Search 100 bp 5'
Search 100 bp 3'