Canonical Allele Identifier: CA2079394615

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24884083T= , CM000675.2:g.24884083T=	GRCh38
NC_000013.10:g.25458221T= , CM000675.1:g.25458221T=	GRCh37
NC_000013.9:g.24356221T=	NCBI36
NG_009165.2:g.43865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.3704A= (CENPJ) MANE Select	ENSP00000371308.4:p.Glu1235=
ENST00000545981.6:c.*444A= (CENPJ)	ENSP00000441090.2:n.*444A=
ENST00000381884.8:c.3704A= (CENPJ)	ENSP00000371308.4:p.Glu1235=
ENST00000545981.5:c.*445A= (CENPJ)	ENSP00000441090.2:n.*445A=
ENST00000616936.4:c.*358A= (CENPJ)	ENSP00000477511.1:n.*358A=
NM_018451.4:c.3704A= (CENPJ)	NP_060921.3:p.Glu1235=
NR_047594.1:n.4016A= (CENPJ)
NR_047595.1:n.3814A= (CENPJ)
XM_011535156.1:c.*11-4031T= (RNF17)	XP_011533458.1:n.*11-4031T=
XM_011535156.2:c.*11-4031T= (RNF17)	XP_011533458.1:n.*11-4031T=
NM_018451.5:c.3704A= (CENPJ) MANE Select	NP_060921.3:p.Glu1235=
NR_047594.2:n.3988A= (CENPJ)
NR_047595.2:n.3786A= (CENPJ)