Canonical Allele Identifier: CA2079394003

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882963T= , CM000675.2:g.24882963T=	GRCh38
NC_000013.10:g.25457101T= , CM000675.1:g.25457101T=	GRCh37
NC_000013.9:g.24355101T=	NCBI36
NG_009165.2:g.44985A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*214A= (CENPJ) MANE Select	ENSP00000371308.4:n.*214A=
ENST00000616936.4:c.*885A= (CENPJ)	ENSP00000477511.1:n.*885A=
NM_018451.4:c.*214A= (CENPJ)	NP_060921.3:n.*214A=
NR_047594.1:n.4543A= (CENPJ)
NR_047595.1:n.4341A= (CENPJ)
XM_011535156.1:c.*10+3668T= (RNF17)	XP_011533458.1:n.*10+3668T=
XM_011535156.2:c.*10+3668T= (RNF17)	XP_011533458.1:n.*10+3668T=
NM_018451.5:c.*214A= (CENPJ) MANE Select	NP_060921.3:n.*214A=
NR_047594.2:n.4515A= (CENPJ)
NR_047595.2:n.4313A= (CENPJ)