Canonical Allele Identifier: CA696759410
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs1239339007
MyVariant Identifiers: chr13:g.25457011G>A (hg19) chr13:g.24882873G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882873G>A , CM000675.2:g.24882873G>A GRCh38
NC_000013.10:g.25457011G>A , CM000675.1:g.25457011G>A GRCh37
NC_000013.9:g.24355011G>A NCBI36
NG_009165.2:g.45075C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*304C>T (CENPJ) MANE Select ENSP00000371308.4:n.*304C>T
ENST00000616936.4:c.*975C>T (CENPJ) ENSP00000477511.1:n.*975C>T
NM_018451.4:c.*304C>T (CENPJ) NP_060921.3:n.*304C>T
NR_047594.1:n.4633C>T (CENPJ)
NR_047595.1:n.4431C>T (CENPJ)
XM_011535156.1:c.*10+3578G>A (RNF17) XP_011533458.1:n.*10+3578G>A
XM_011535156.2:c.*10+3578G>A (RNF17) XP_011533458.1:n.*10+3578G>A
NM_018451.5:c.*304C>T (CENPJ) MANE Select NP_060921.3:n.*304C>T
NR_047594.2:n.4605C>T (CENPJ)
NR_047595.2:n.4403C>T (CENPJ)
Search 100 bp 5'
Search 100 bp 3'