Canonical Allele Identifier: CA2079394126

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883167A= , CM000675.2:g.24883167A=	GRCh38
NC_000013.10:g.25457305A= , CM000675.1:g.25457305A=	GRCh37
NC_000013.9:g.24355305A=	NCBI36
NG_009165.2:g.44781T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.*10T= (CENPJ) MANE Select	ENSP00000371308.4:n.*10T=
ENST00000545981.6:c.*767T= (CENPJ)	ENSP00000441090.2:n.*767T=
ENST00000381884.8:c.*10T= (CENPJ)	ENSP00000371308.4:n.*10T=
ENST00000545981.5:c.*768T= (CENPJ)	ENSP00000441090.2:n.*768T=
ENST00000616936.4:c.*681T= (CENPJ)	ENSP00000477511.1:n.*681T=
NM_018451.4:c.*10T= (CENPJ)	NP_060921.3:n.*10T=
NR_047594.1:n.4339T= (CENPJ)
NR_047595.1:n.4137T= (CENPJ)
XM_011535156.1:c.*10+3872A= (RNF17)	XP_011533458.1:n.*10+3872A=
XM_011535156.2:c.*10+3872A= (RNF17)	XP_011533458.1:n.*10+3872A=
NM_018451.5:c.*10T= (CENPJ) MANE Select	NP_060921.3:n.*10T=
NR_047594.2:n.4311T= (CENPJ)
NR_047595.2:n.4109T= (CENPJ)