Canonical Allele Identifier: CA2079394182

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883260C= , CM000675.2:g.24883260C=	GRCh38
NC_000013.10:g.25457398C= , CM000675.1:g.25457398C=	GRCh37
NC_000013.9:g.24355398C=	NCBI36
NG_009165.2:g.44688G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3934G= (CENPJ) MANE Select	ENSP00000371308.4:p.Gly1312=
ENST00000545981.6:c.*674G= (CENPJ)	ENSP00000441090.2:n.*674G=
ENST00000381884.8:c.3934G= (CENPJ)	ENSP00000371308.4:p.Gly1312=
ENST00000545981.5:c.*675G= (CENPJ)	ENSP00000441090.2:n.*675G=
ENST00000616936.4:c.*588G= (CENPJ)	ENSP00000477511.1:n.*588G=
NM_018451.4:c.3934G= (CENPJ)	NP_060921.3:p.Gly1312=
NR_047594.1:n.4246G= (CENPJ)
NR_047595.1:n.4044G= (CENPJ)
XM_011535156.1:c.*10+3965C= (RNF17)	XP_011533458.1:n.*10+3965C=
XM_011535156.2:c.*10+3965C= (RNF17)	XP_011533458.1:n.*10+3965C=
NM_018451.5:c.3934G= (CENPJ) MANE Select	NP_060921.3:p.Gly1312=
NR_047594.2:n.4218G= (CENPJ)
NR_047595.2:n.4016G= (CENPJ)