Canonical Allele Identifier: CA2079393952

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882874_24882878delinsGTTTT , CM000675.2:g.24882874_24882878delinsGTTTT	GRCh38
NC_000013.10:g.25457012_25457016delinsGTTTT , CM000675.1:g.25457012_25457016delinsGTTTT	GRCh37
NC_000013.9:g.24355012_24355016delinsGTTTT	NCBI36
NG_009165.2:g.45070_45074delinsAAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*299_*303delinsAAAAC (CENPJ) MANE Select	ENSP00000371308.4:n.*299_*303delinsAAAAC
ENST00000616936.4:c.*970_*974delinsAAAAC (CENPJ)	ENSP00000477511.1:n.*970_*974delinsAAAAC
NM_018451.4:c.*299_*303delinsAAAAC (CENPJ)	NP_060921.3:n.*299_*303delinsAAAAC
NR_047594.1:n.4628_4632delinsAAAAC (CENPJ)
NR_047595.1:n.4426_4430delinsAAAAC (CENPJ)
XM_011535156.1:c.*10+3579_*10+3583delinsGTTTT (RNF17)	XP_011533458.1:n.*10+3579_*10+3583delinsGTTTT
XM_011535156.2:c.*10+3579_*10+3583delinsGTTTT (RNF17)	XP_011533458.1:n.*10+3579_*10+3583delinsGTTTT
NM_018451.5:c.*299_*303delinsAAAAC (CENPJ) MANE Select	NP_060921.3:n.*299_*303delinsAAAAC
NR_047594.2:n.4600_4604delinsAAAAC (CENPJ)
NR_047595.2:n.4398_4402delinsAAAAC (CENPJ)