Canonical Allele Identifier: CA2622386623

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883087_24883092del , CM000675.2:g.24883087_24883092del GRCh38
NC_000013.10:g.25457225_25457230del , CM000675.1:g.25457225_25457230del GRCh37
NC_000013.9:g.24355225_24355230del NCBI36
NG_009165.2:g.44861_44866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*90_*95del (CENPJ) MANE Select ENSP00000371308.4:n.*90_*95del
ENST00000381884.8:c.*90_*95del (CENPJ) ENSP00000371308.4:n.*90_*95del
ENST00000616936.4:c.*761_*766del (CENPJ) ENSP00000477511.1:n.*761_*766del
NM_018451.4:c.*90_*95del (CENPJ) NP_060921.3:n.*90_*95del
NR_047594.1:n.4419_4424del (CENPJ)
NR_047595.1:n.4217_4222del (CENPJ)
XM_011535156.1:c.*10+3792_*10+3797del (RNF17) XP_011533458.1:n.*10+3792_*10+3797del
XM_011535156.2:c.*10+3792_*10+3797del (RNF17) XP_011533458.1:n.*10+3792_*10+3797del
NM_018451.5:c.*90_*95del (CENPJ) MANE Select NP_060921.3:n.*90_*95del
NR_047594.2:n.4391_4396del (CENPJ)
NR_047595.2:n.4189_4194del (CENPJ)