Canonical Allele Identifier: CA482981537
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

gnomAD v4: 13-24883255-A-G
MyVariant Identifiers: chr13:g.25457393A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883255A>G , CM000675.2:g.24883255A>G GRCh38
NC_000013.10:g.25457393A>G , CM000675.1:g.25457393A>G GRCh37
NC_000013.9:g.24355393A>G NCBI36
NG_009165.2:g.44693T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3939T>C (CENPJ) MANE Select ENSP00000371308.4:p.His1313=
ENST00000545981.6:c.*679T>C (CENPJ) ENSP00000441090.2:n.*679T>C
ENST00000381884.8:c.3939T>C (CENPJ) ENSP00000371308.4:p.His1313=
ENST00000545981.5:c.*680T>C (CENPJ) ENSP00000441090.2:n.*680T>C
ENST00000616936.4:c.*593T>C (CENPJ) ENSP00000477511.1:n.*593T>C
NM_018451.4:c.3939T>C (CENPJ) NP_060921.3:p.His1313=
NR_047594.1:n.4251T>C (CENPJ)
NR_047595.1:n.4049T>C (CENPJ)
XM_011535156.1:c.*10+3960A>G (RNF17) XP_011533458.1:n.*10+3960A>G
XM_011535156.2:c.*10+3960A>G (RNF17) XP_011533458.1:n.*10+3960A>G
NM_018451.5:c.3939T>C (CENPJ) MANE Select NP_060921.3:p.His1313=
NR_047594.2:n.4223T>C (CENPJ)
NR_047595.2:n.4021T>C (CENPJ)
Search 100 bp 5'
Search 100 bp 3'