Canonical Allele Identifier: CA2079382529

Gene: CENPJ

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24905686T= , CM000675.2:g.24905686T=	GRCh38
NC_000013.10:g.25479824T= , CM000675.1:g.25479824T=	GRCh37
NC_000013.9:g.24377824T=	NCBI36
NG_009165.2:g.22262A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.2352A= MANE Select	ENSP00000371308.4:p.Ser784=
ENST00000545981.6:c.2352A=	ENSP00000441090.2:p.Ser784=
ENST00000381884.8:c.2352A=	ENSP00000371308.4:p.Ser784=
ENST00000545981.5:c.2352A=	ENSP00000441090.2:p.Ser784=
ENST00000616936.4:c.2352A=	ENSP00000477511.1:p.Ser784=
NM_018451.4:c.2352A=	NP_060921.3:p.Ser784=
NR_047594.1:n.2547A=
NR_047595.1:n.2547A=
XM_011535149.1:c.2352A=	XP_011533451.1:p.Ser784=
XM_011535150.1:c.2352A=	XP_011533452.1:p.Ser784=
XM_011535151.1:c.2352A=	XP_011533453.1:p.Ser784=
XR_941627.1:n.2547A=
XR_941628.1:n.2547A=
XM_011535149.2:c.2352A=	XP_011533451.1:p.Ser784=
XM_011535150.2:c.2352A=	XP_011533452.1:p.Ser784=
XM_017020673.1:c.2352A=	XP_016876162.1:p.Ser784=
NM_018451.5:c.2352A= MANE Select	NP_060921.3:p.Ser784=
NR_047594.2:n.2519A=
NR_047595.2:n.2519A=