Canonical Allele Identifier: CA6919056
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs577663382
ExAC: 13:25457271 C / T
gnomAD v2: 13-25457271-C-T
gnomAD v3: 13-24883133-C-T
gnomAD v4: 13-24883133-C-T
MyVariant Identifiers: chr13:g.25457271C>T (hg19) chr13:g.25457271_25457273delinsTAT (hg19) chr13:g.24883133C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883133C>T , CM000675.2:g.24883133C>T GRCh38
NC_000013.10:g.25457271C>T , CM000675.1:g.25457271C>T GRCh37
NC_000013.9:g.24355271C>T NCBI36
NG_009165.2:g.44815G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*44G>A (CENPJ) MANE Select ENSP00000371308.4:n.*44G>A
ENST00000381884.8:c.*44G>A (CENPJ) ENSP00000371308.4:n.*44G>A
ENST00000616936.4:c.*715G>A (CENPJ) ENSP00000477511.1:n.*715G>A
NM_018451.4:c.*44G>A (CENPJ) NP_060921.3:n.*44G>A
NR_047594.1:n.4373G>A (CENPJ)
NR_047595.1:n.4171G>A (CENPJ)
XM_011535156.1:c.*10+3838C>T (RNF17) XP_011533458.1:n.*10+3838C>T
XM_011535156.2:c.*10+3838C>T (RNF17) XP_011533458.1:n.*10+3838C>T
NM_018451.5:c.*44G>A (CENPJ) MANE Select NP_060921.3:n.*44G>A
NR_047594.2:n.4345G>A (CENPJ)
NR_047595.2:n.4143G>A (CENPJ)
Search 100 bp 5'
Search 100 bp 3'