Canonical Allele Identifier: CA2079394082

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883108_24883109delinsTC , CM000675.2:g.24883108_24883109delinsTC	GRCh38
NC_000013.10:g.25457246_25457247delinsTC , CM000675.1:g.25457246_25457247delinsTC	GRCh37
NC_000013.9:g.24355246_24355247delinsTC	NCBI36
NG_009165.2:g.44839_44840delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*68_*69delinsGA (CENPJ) MANE Select	ENSP00000371308.4:n.*68_*69delinsGA
ENST00000381884.8:c.*68_*69delinsGA (CENPJ)	ENSP00000371308.4:n.*68_*69delinsGA
ENST00000616936.4:c.*739_*740delinsGA (CENPJ)	ENSP00000477511.1:n.*739_*740delinsGA
NM_018451.4:c.*68_*69delinsGA (CENPJ)	NP_060921.3:n.*68_*69delinsGA
NR_047594.1:n.4397_4398delinsGA (CENPJ)
NR_047595.1:n.4195_4196delinsGA (CENPJ)
XM_011535156.1:c.*10+3813_*10+3814delinsTC (RNF17)	XP_011533458.1:n.*10+3813_*10+3814delinsTC
XM_011535156.2:c.*10+3813_*10+3814delinsTC (RNF17)	XP_011533458.1:n.*10+3813_*10+3814delinsTC
NM_018451.5:c.*68_*69delinsGA (CENPJ) MANE Select	NP_060921.3:n.*68_*69delinsGA
NR_047594.2:n.4369_4370delinsGA (CENPJ)
NR_047595.2:n.4167_4168delinsGA (CENPJ)