Canonical Allele Identifier: CA2622386679
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

gnomAD v4: 13-24883166-CAT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883167_24883168del , CM000675.2:g.24883167_24883168del GRCh38
NC_000013.10:g.25457305_25457306del , CM000675.1:g.25457305_25457306del GRCh37
NC_000013.9:g.24355305_24355306del NCBI36
NG_009165.2:g.44780_44781del

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.*9_*10del (CENPJ) MANE Select ENSP00000371308.4:n.*9_*10del
ENST00000545981.6:c.*766_*767del (CENPJ) ENSP00000441090.2:n.*766_*767del
ENST00000381884.8:c.*9_*10del (CENPJ) ENSP00000371308.4:n.*9_*10del
ENST00000545981.5:c.*767_*768del (CENPJ) ENSP00000441090.2:n.*767_*768del
ENST00000616936.4:c.*680_*681del (CENPJ) ENSP00000477511.1:n.*680_*681del
NM_018451.4:c.*9_*10del (CENPJ) NP_060921.3:n.*9_*10del
NR_047594.1:n.4338_4339del (CENPJ)
NR_047595.1:n.4136_4137del (CENPJ)
XM_011535156.1:c.*10+3872_*10+3873del (RNF17) XP_011533458.1:n.*10+3872_*10+3873del
XM_011535156.2:c.*10+3872_*10+3873del (RNF17) XP_011533458.1:n.*10+3872_*10+3873del
NM_018451.5:c.*9_*10del (CENPJ) MANE Select NP_060921.3:n.*9_*10del
NR_047594.2:n.4310_4311del (CENPJ)
NR_047595.2:n.4108_4109del (CENPJ)
Search 100 bp 5'
Search 100 bp 3'