Canonical Allele Identifier: CA954159575

Linked Data

dbSNP Id: rs1953904827

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882995_24882998del , CM000675.2:g.24882995_24882998del GRCh38
NC_000013.10:g.25457133_25457136del , CM000675.1:g.25457133_25457136del GRCh37
NC_000013.9:g.24355133_24355136del NCBI36
NG_009165.2:g.44952_44955del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*181_*184del (CENPJ) MANE Select ENSP00000371308.4:n.*181_*184del
ENST00000616936.4:c.*852_*855del (CENPJ) ENSP00000477511.1:n.*852_*855del
NM_018451.4:c.*181_*184del (CENPJ) NP_060921.3:n.*181_*184del
NR_047594.1:n.4510_4513del (CENPJ)
NR_047595.1:n.4308_4311del (CENPJ)
XM_011535156.1:c.*10+3700_*10+3703del (RNF17) XP_011533458.1:n.*10+3700_*10+3703del
XM_011535156.2:c.*10+3700_*10+3703del (RNF17) XP_011533458.1:n.*10+3700_*10+3703del
NM_018451.5:c.*181_*184del (CENPJ) MANE Select NP_060921.3:n.*181_*184del
NR_047594.2:n.4482_4485del (CENPJ)
NR_047595.2:n.4280_4283del (CENPJ)