Canonical Allele Identifier: CA2079394042

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883054_24883058delinsTTTTA , CM000675.2:g.24883054_24883058delinsTTTTA	GRCh38
NC_000013.10:g.25457192_25457196delinsTTTTA , CM000675.1:g.25457192_25457196delinsTTTTA	GRCh37
NC_000013.9:g.24355192_24355196delinsTTTTA	NCBI36
NG_009165.2:g.44890_44894delinsTAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*119_*123delinsTAAAA (CENPJ) MANE Select	ENSP00000371308.4:n.*119_*123delinsTAAAA
ENST00000381884.8:c.*119_*123delinsTAAAA (CENPJ)	ENSP00000371308.4:n.*119_*123delinsTAAAA
ENST00000616936.4:c.*790_*794delinsTAAAA (CENPJ)	ENSP00000477511.1:n.*790_*794delinsTAAAA
NM_018451.4:c.*119_*123delinsTAAAA (CENPJ)	NP_060921.3:n.*119_*123delinsTAAAA
NR_047594.1:n.4448_4452delinsTAAAA (CENPJ)
NR_047595.1:n.4246_4250delinsTAAAA (CENPJ)
XM_011535156.1:c.*10+3759_*10+3763delinsTTTTA (RNF17)	XP_011533458.1:n.*10+3759_*10+3763delinsTTTTA
XM_011535156.2:c.*10+3759_*10+3763delinsTTTTA (RNF17)	XP_011533458.1:n.*10+3759_*10+3763delinsTTTTA
NM_018451.5:c.*119_*123delinsTAAAA (CENPJ) MANE Select	NP_060921.3:n.*119_*123delinsTAAAA
NR_047594.2:n.4420_4424delinsTAAAA (CENPJ)
NR_047595.2:n.4218_4222delinsTAAAA (CENPJ)