Canonical Allele Identifier: CA2079394206

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883315G= , CM000675.2:g.24883315G=	GRCh38
NC_000013.10:g.25457453G= , CM000675.1:g.25457453G=	GRCh37
NC_000013.9:g.24355453G=	NCBI36
NG_009165.2:g.44633C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.3879C= (CENPJ) MANE Select	ENSP00000371308.4:p.Ala1293=
ENST00000545981.6:c.*619C= (CENPJ)	ENSP00000441090.2:n.*619C=
ENST00000381884.8:c.3879C= (CENPJ)	ENSP00000371308.4:p.Ala1293=
ENST00000545981.5:c.*620C= (CENPJ)	ENSP00000441090.2:n.*620C=
ENST00000616936.4:c.*533C= (CENPJ)	ENSP00000477511.1:n.*533C=
NM_018451.4:c.3879C= (CENPJ)	NP_060921.3:p.Ala1293=
NR_047594.1:n.4191C= (CENPJ)
NR_047595.1:n.3989C= (CENPJ)
XM_011535156.1:c.*10+4020G= (RNF17)	XP_011533458.1:n.*10+4020G=
XM_011535156.2:c.*10+4020G= (RNF17)	XP_011533458.1:n.*10+4020G=
NM_018451.5:c.3879C= (CENPJ) MANE Select	NP_060921.3:p.Ala1293=
NR_047594.2:n.4163C= (CENPJ)
NR_047595.2:n.3961C= (CENPJ)