Canonical Allele Identifier: CA954159577
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs1953905034
gnomAD v3: 13-24883003-G-A
gnomAD v4: 13-24883003-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883003G>A , CM000675.2:g.24883003G>A GRCh38
NC_000013.10:g.25457141G>A , CM000675.1:g.25457141G>A GRCh37
NC_000013.9:g.24355141G>A NCBI36
NG_009165.2:g.44945C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*174C>T (CENPJ) MANE Select ENSP00000371308.4:n.*174C>T
ENST00000616936.4:c.*845C>T (CENPJ) ENSP00000477511.1:n.*845C>T
NM_018451.4:c.*174C>T (CENPJ) NP_060921.3:n.*174C>T
NR_047594.1:n.4503C>T (CENPJ)
NR_047595.1:n.4301C>T (CENPJ)
XM_011535156.1:c.*10+3708G>A (RNF17) XP_011533458.1:n.*10+3708G>A
XM_011535156.2:c.*10+3708G>A (RNF17) XP_011533458.1:n.*10+3708G>A
NM_018451.5:c.*174C>T (CENPJ) MANE Select NP_060921.3:n.*174C>T
NR_047594.2:n.4475C>T (CENPJ)
NR_047595.2:n.4273C>T (CENPJ)
Search 100 bp 5'
Search 100 bp 3'