Canonical Allele Identifier: CA10639281
Gene: CENPJ HGNC NCBI

Linked Data

ClinVar Variation Id: 311630
dbSNP Id: rs886050101

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24912010T>C , CM000675.2:g.24912010T>C GRCh38
NC_000013.10:g.25486148T>C , CM000675.1:g.25486148T>C GRCh37
NC_000013.9:g.24384148T>C NCBI36
NG_009165.2:g.15938A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.504A>G MANE Select ENSP00000371308.4:p.Leu168=
ENST00000545981.6:c.504A>G ENSP00000441090.2:p.Leu168=
ENST00000381884.8:c.504A>G ENSP00000371308.4:p.Leu168=
ENST00000545981.5:c.504A>G ENSP00000441090.2:p.Leu168=
ENST00000616936.4:c.504A>G ENSP00000477511.1:p.Leu168=
NM_018451.4:c.504A>G NP_060921.3:p.Leu168=
NR_047594.1:n.699A>G
NR_047595.1:n.699A>G
XM_011535149.1:c.504A>G XP_011533451.1:p.Leu168=
XM_011535150.1:c.504A>G XP_011533452.1:p.Leu168=
XM_011535151.1:c.504A>G XP_011533453.1:p.Leu168=
XR_941627.1:n.699A>G
XR_941628.1:n.699A>G
XM_011535149.2:c.504A>G XP_011533451.1:p.Leu168=
XM_011535150.2:c.504A>G XP_011533452.1:p.Leu168=
XM_017020673.1:c.504A>G XP_016876162.1:p.Leu168=
NM_018451.5:c.504A>G MANE Select NP_060921.3:p.Leu168=
NR_047594.2:n.671A>G
NR_047595.2:n.671A>G