Canonical Allele Identifier: CA2079393934

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882862_24882871delinsCTGTACTTCT , CM000675.2:g.24882862_24882871delinsCTGTACTTCT GRCh38
NC_000013.10:g.25457000_25457009delinsCTGTACTTCT , CM000675.1:g.25457000_25457009delinsCTGTACTTCT GRCh37
NC_000013.9:g.24355000_24355009delinsCTGTACTTCT NCBI36
NG_009165.2:g.45077_45086delinsAGAAGTACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*306_*315delinsAGAAGTACAG (CENPJ) MANE Select ENSP00000371308.4:n.*306_*315delinsAGAAGTACAG
ENST00000616936.4:c.*977_*986delinsAGAAGTACAG (CENPJ) ENSP00000477511.1:n.*977_*986delinsAGAAGTACAG
NM_018451.4:c.*306_*315delinsAGAAGTACAG (CENPJ) NP_060921.3:n.*306_*315delinsAGAAGTACAG
NR_047594.1:n.4635_4644delinsAGAAGTACAG (CENPJ)
NR_047595.1:n.4433_4442delinsAGAAGTACAG (CENPJ)
XM_011535156.1:c.*10+3567_*10+3576delinsCTGTACTTCT (RNF17) XP_011533458.1:n.*10+3567_*10+3576delinsCTGTACTTCT
XM_011535156.2:c.*10+3567_*10+3576delinsCTGTACTTCT (RNF17) XP_011533458.1:n.*10+3567_*10+3576delinsCTGTACTTCT
NM_018451.5:c.*306_*315delinsAGAAGTACAG (CENPJ) MANE Select NP_060921.3:n.*306_*315delinsAGAAGTACAG
NR_047594.2:n.4607_4616delinsAGAAGTACAG (CENPJ)
NR_047595.2:n.4405_4414delinsAGAAGTACAG (CENPJ)