Canonical Allele Identifier: CA2622386428
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

gnomAD v4: 13-24882848-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882848A>T , CM000675.2:g.24882848A>T GRCh38
NC_000013.10:g.25456986A>T , CM000675.1:g.25456986A>T GRCh37
NC_000013.9:g.24354986A>T NCBI36
NG_009165.2:g.45100T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*329T>A (CENPJ) MANE Select ENSP00000371308.4:n.*329T>A
ENST00000616936.4:c.*1000T>A (CENPJ) ENSP00000477511.1:n.*1000T>A
NM_018451.4:c.*329T>A (CENPJ) NP_060921.3:n.*329T>A
NR_047594.1:n.4658T>A (CENPJ)
NR_047595.1:n.4456T>A (CENPJ)
XM_011535156.1:c.*10+3553A>T (RNF17) XP_011533458.1:n.*10+3553A>T
XM_011535156.2:c.*10+3553A>T (RNF17) XP_011533458.1:n.*10+3553A>T
NM_018451.5:c.*329T>A (CENPJ) MANE Select NP_060921.3:n.*329T>A
NR_047594.2:n.4630T>A (CENPJ)
NR_047595.2:n.4428T>A (CENPJ)
Search 100 bp 5'
Search 100 bp 3'