Canonical Allele Identifier: CA396008068
Gene: CETP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983344C>A , CM000678.2:g.56983344C>A GRCh38
NC_000016.9:g.57017256C>A , CM000678.1:g.57017256C>A GRCh37
NC_000016.8:g.55574757C>A NCBI36
NG_008952.1:g.26422C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1340C>A MANE Select ENSP00000200676.3:p.Thr447Lys
ENST00000650358.1:n.1738C>A
ENST00000200676.7:c.1340C>A ENSP00000200676.3:p.Thr447Lys
ENST00000379780.6:c.1160C>A ENSP00000369106.2:p.Thr387Lys
ENST00000566128.1:c.1145C>A ENSP00000456276.1:p.Thr382Lys
NM_000078.2:c.1340C>A NP_000069.2:p.Thr447Lys
NM_001286085.1:c.1160C>A NP_001273014.1:p.Thr387Lys
NM_000078.3:c.1340C>A MANE Select NP_000069.2:p.Thr447Lys
NM_001286085.2:c.1160C>A NP_001273014.1:p.Thr387Lys