Canonical Allele Identifier: CA483169032

Gene: CENPJ

Linked Data

• MyVariant Identifiers: chr13:g.25479722A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24905584A>C , CM000675.2:g.24905584A>C	GRCh38
NC_000013.10:g.25479722A>C , CM000675.1:g.25479722A>C	GRCh37
NC_000013.9:g.24377722A>C	NCBI36
NG_009165.2:g.22364T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.2454T>G MANE Select	ENSP00000371308.4:p.Thr818=
ENST00000545981.6:c.2454T>G	ENSP00000441090.2:p.Thr818=
ENST00000381884.8:c.2454T>G	ENSP00000371308.4:p.Thr818=
ENST00000545981.5:c.2454T>G	ENSP00000441090.2:p.Thr818=
ENST00000616936.4:c.2454T>G	ENSP00000477511.1:p.Thr818=
NM_018451.4:c.2454T>G	NP_060921.3:p.Thr818=
NR_047594.1:n.2649T>G
NR_047595.1:n.2649T>G
XM_011535149.1:c.2454T>G	XP_011533451.1:p.Thr818=
XM_011535150.1:c.2454T>G	XP_011533452.1:p.Thr818=
XM_011535151.1:c.2454T>G	XP_011533453.1:p.Thr818=
XR_941627.1:n.2649T>G
XR_941628.1:n.2649T>G
XM_011535149.2:c.2454T>G	XP_011533451.1:p.Thr818=
XM_011535150.2:c.2454T>G	XP_011533452.1:p.Thr818=
XM_017020673.1:c.2454T>G	XP_016876162.1:p.Thr818=
NM_018451.5:c.2454T>G MANE Select	NP_060921.3:p.Thr818=
NR_047594.2:n.2621T>G
NR_047595.2:n.2621T>G