Canonical Allele Identifier: CA2798539589

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882883_24882884insTTTTTTTTTTTTT , CM000675.2:g.24882883_24882884insTTTTTTTTTTTTT GRCh38
NC_000013.10:g.25457021_25457022insTTTTTTTTTTTTT , CM000675.1:g.25457021_25457022insTTTTTTTTTTTTT GRCh37
NC_000013.9:g.24355021_24355022insTTTTTTTTTTTTT NCBI36
NG_009165.2:g.45073_45074insAAAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*302_*303insAAAAAAAAAAAAA (CENPJ) MANE Select ENSP00000371308.4:n.*302_*303insAAAAAAAAAAAAA
ENST00000616936.4:c.*973_*974insAAAAAAAAAAAAA (CENPJ) ENSP00000477511.1:n.*973_*974insAAAAAAAAAAAAA
NM_018451.4:c.*302_*303insAAAAAAAAAAAAA (CENPJ) NP_060921.3:n.*302_*303insAAAAAAAAAAAAA
NR_047594.1:n.4631_4632insAAAAAAAAAAAAA (CENPJ)
NR_047595.1:n.4429_4430insAAAAAAAAAAAAA (CENPJ)
XM_011535156.1:c.*10+3588_*10+3589insTTTTTTTTTTTTT (RNF17) XP_011533458.1:n.*10+3588_*10+3589insTTTTTTTTTTTTT
XM_011535156.2:c.*10+3588_*10+3589insTTTTTTTTTTTTT (RNF17) XP_011533458.1:n.*10+3588_*10+3589insTTTTTTTTTTTTT
NM_018451.5:c.*302_*303insAAAAAAAAAAAAA (CENPJ) MANE Select NP_060921.3:n.*302_*303insAAAAAAAAAAAAA
NR_047594.2:n.4603_4604insAAAAAAAAAAAAA (CENPJ)
NR_047595.2:n.4401_4402insAAAAAAAAAAAAA (CENPJ)