Canonical Allele Identifier: CA2079394118

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883153T= , CM000675.2:g.24883153T=	GRCh38
NC_000013.10:g.25457291T= , CM000675.1:g.25457291T=	GRCh37
NC_000013.9:g.24355291T=	NCBI36
NG_009165.2:g.44795A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*24A= (CENPJ) MANE Select	ENSP00000371308.4:n.*24A=
ENST00000381884.8:c.*24A= (CENPJ)	ENSP00000371308.4:n.*24A=
ENST00000616936.4:c.*695A= (CENPJ)	ENSP00000477511.1:n.*695A=
NM_018451.4:c.*24A= (CENPJ)	NP_060921.3:n.*24A=
NR_047594.1:n.4353A= (CENPJ)
NR_047595.1:n.4151A= (CENPJ)
XM_011535156.1:c.*10+3858T= (RNF17)	XP_011533458.1:n.*10+3858T=
XM_011535156.2:c.*10+3858T= (RNF17)	XP_011533458.1:n.*10+3858T=
NM_018451.5:c.*24A= (CENPJ) MANE Select	NP_060921.3:n.*24A=
NR_047594.2:n.4325A= (CENPJ)
NR_047595.2:n.4123A= (CENPJ)