Canonical Allele Identifier: CA2079393957

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882876T= , CM000675.2:g.24882876T=	GRCh38
NC_000013.10:g.25457014T= , CM000675.1:g.25457014T=	GRCh37
NC_000013.9:g.24355014T=	NCBI36
NG_009165.2:g.45072A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*301A= (CENPJ) MANE Select	ENSP00000371308.4:n.*301A=
ENST00000616936.4:c.*972A= (CENPJ)	ENSP00000477511.1:n.*972A=
NM_018451.4:c.*301A= (CENPJ)	NP_060921.3:n.*301A=
NR_047594.1:n.4630A= (CENPJ)
NR_047595.1:n.4428A= (CENPJ)
XM_011535156.1:c.*10+3581T= (RNF17)	XP_011533458.1:n.*10+3581T=
XM_011535156.2:c.*10+3581T= (RNF17)	XP_011533458.1:n.*10+3581T=
NM_018451.5:c.*301A= (CENPJ) MANE Select	NP_060921.3:n.*301A=
NR_047594.2:n.4602A= (CENPJ)
NR_047595.2:n.4400A= (CENPJ)