Canonical Allele Identifier: CA696759544
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs9318911
gnomAD v4: 13-24883069-T-A
MyVariant Identifiers: chr13:g.25457207T>A (hg19) chr13:g.24883069T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883069T>A , CM000675.2:g.24883069T>A GRCh38
NC_000013.10:g.25457207T>A , CM000675.1:g.25457207T>A GRCh37
NC_000013.9:g.24355207T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*108A>T (CENPJ) MANE Select ENSP00000371308.4:n.*108A>T
ENST00000381884.8:c.*108A>T (CENPJ) ENSP00000371308.4:n.*108A>T
ENST00000616936.4:c.*779A>T (CENPJ) ENSP00000477511.1:n.*779A>T
XM_011535156.1:c.*10+3774T>A (RNF17) XP_011533458.1:n.*10+3774T>A
XM_011535156.2:c.*10+3774T>A (RNF17) XP_011533458.1:n.*10+3774T>A
NM_018451.5:c.*108A>T (CENPJ) MANE Select NP_060921.3:n.*108A>T
NR_047594.2:n.4409A>T (CENPJ)
NR_047595.2:n.4207A>T (CENPJ)
Search 100 bp 5'
Search 100 bp 3'