Canonical Allele Identifier: CA2079394076
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs1359925138
gnomAD v4: 13-24883103-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883103C>T , CM000675.2:g.24883103C>T GRCh38
NC_000013.10:g.25457241C>T , CM000675.1:g.25457241C>T GRCh37
NC_000013.9:g.24355241C>T NCBI36
NG_009165.2:g.44845G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*74G>A (CENPJ) MANE Select ENSP00000371308.4:n.*74G>A
ENST00000381884.8:c.*74G>A (CENPJ) ENSP00000371308.4:n.*74G>A
ENST00000616936.4:c.*745G>A (CENPJ) ENSP00000477511.1:n.*745G>A
NM_018451.4:c.*74G>A (CENPJ) NP_060921.3:n.*74G>A
NR_047594.1:n.4403G>A (CENPJ)
NR_047595.1:n.4201G>A (CENPJ)
XM_011535156.1:c.*10+3808C>T (RNF17) XP_011533458.1:n.*10+3808C>T
XM_011535156.2:c.*10+3808C>T (RNF17) XP_011533458.1:n.*10+3808C>T
NM_018451.5:c.*74G>A (CENPJ) MANE Select NP_060921.3:n.*74G>A
NR_047594.2:n.4375G>A (CENPJ)
NR_047595.2:n.4173G>A (CENPJ)
Search 100 bp 5'
Search 100 bp 3'