Canonical Allele Identifier: CA913805060
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs1566274960
gnomAD v2: 13-25457282-AGTTACT-A
gnomAD v3: 13-24883144-AGTTACT-A
gnomAD v4: 13-24883144-AGTTACT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883151_24883156del , CM000675.2:g.24883151_24883156del GRCh38
NC_000013.10:g.25457289_25457294del , CM000675.1:g.25457289_25457294del GRCh37
NC_000013.9:g.24355289_24355294del NCBI36
NG_009165.2:g.44798_44803del

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.*27_*32del (CENPJ) MANE Select ENSP00000371308.4:n.*27_*32del
ENST00000381884.8:c.*27_*32del (CENPJ) ENSP00000371308.4:n.*27_*32del
ENST00000616936.4:c.*698_*703del (CENPJ) ENSP00000477511.1:n.*698_*703del
NM_018451.4:c.*27_*32del (CENPJ) NP_060921.3:n.*27_*32del
NR_047594.1:n.4356_4361del (CENPJ)
NR_047595.1:n.4154_4159del (CENPJ)
XM_011535156.1:c.*10+3856_*10+3861del (RNF17) XP_011533458.1:n.*10+3856_*10+3861del
XM_011535156.2:c.*10+3856_*10+3861del (RNF17) XP_011533458.1:n.*10+3856_*10+3861del
NM_018451.5:c.*27_*32del (CENPJ) MANE Select NP_060921.3:n.*27_*32del
NR_047594.2:n.4328_4333del (CENPJ)
NR_047595.2:n.4126_4131del (CENPJ)
Search 100 bp 5'
Search 100 bp 3'