Canonical Allele Identifier: CA2079394008

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882975_24882979delinsAAGAC , CM000675.2:g.24882975_24882979delinsAAGAC	GRCh38
NC_000013.10:g.25457113_25457117delinsAAGAC , CM000675.1:g.25457113_25457117delinsAAGAC	GRCh37
NC_000013.9:g.24355113_24355117delinsAAGAC	NCBI36
NG_009165.2:g.44969_44973delinsGTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*198_*202delinsGTCTT (CENPJ) MANE Select	ENSP00000371308.4:n.*198_*202delinsGTCTT
ENST00000616936.4:c.*869_*873delinsGTCTT (CENPJ)	ENSP00000477511.1:n.*869_*873delinsGTCTT
NM_018451.4:c.*198_*202delinsGTCTT (CENPJ)	NP_060921.3:n.*198_*202delinsGTCTT
NR_047594.1:n.4527_4531delinsGTCTT (CENPJ)
NR_047595.1:n.4325_4329delinsGTCTT (CENPJ)
XM_011535156.1:c.*10+3680_*10+3684delinsAAGAC (RNF17)	XP_011533458.1:n.*10+3680_*10+3684delinsAAGAC
XM_011535156.2:c.*10+3680_*10+3684delinsAAGAC (RNF17)	XP_011533458.1:n.*10+3680_*10+3684delinsAAGAC
NM_018451.5:c.*198_*202delinsGTCTT (CENPJ) MANE Select	NP_060921.3:n.*198_*202delinsGTCTT
NR_047594.2:n.4499_4503delinsGTCTT (CENPJ)
NR_047595.2:n.4297_4301delinsGTCTT (CENPJ)