Canonical Allele Identifier: CA2079394127

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883168T= , CM000675.2:g.24883168T=	GRCh38
NC_000013.10:g.25457306T= , CM000675.1:g.25457306T=	GRCh37
NC_000013.9:g.24355306T=	NCBI36
NG_009165.2:g.44780A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.*9A= (CENPJ) MANE Select	ENSP00000371308.4:n.*9A=
ENST00000545981.6:c.*766A= (CENPJ)	ENSP00000441090.2:n.*766A=
ENST00000381884.8:c.*9A= (CENPJ)	ENSP00000371308.4:n.*9A=
ENST00000545981.5:c.*767A= (CENPJ)	ENSP00000441090.2:n.*767A=
ENST00000616936.4:c.*680A= (CENPJ)	ENSP00000477511.1:n.*680A=
NM_018451.4:c.*9A= (CENPJ)	NP_060921.3:n.*9A=
NR_047594.1:n.4338A= (CENPJ)
NR_047595.1:n.4136A= (CENPJ)
XM_011535156.1:c.*10+3873T= (RNF17)	XP_011533458.1:n.*10+3873T=
XM_011535156.2:c.*10+3873T= (RNF17)	XP_011533458.1:n.*10+3873T=
NM_018451.5:c.*9A= (CENPJ) MANE Select	NP_060921.3:n.*9A=
NR_047594.2:n.4310A= (CENPJ)
NR_047595.2:n.4108A= (CENPJ)