Canonical Allele Identifier: CA396008251
Gene: CETP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983376T>G , CM000678.2:g.56983376T>G GRCh38
NC_000016.9:g.57017288T>G , CM000678.1:g.57017288T>G GRCh37
NC_000016.8:g.55574789T>G NCBI36
NG_008952.1:g.26454T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1372T>G MANE Select ENSP00000200676.3:p.Phe458Val
ENST00000650358.1:n.1770T>G
ENST00000200676.7:c.1372T>G ENSP00000200676.3:p.Phe458Val
ENST00000379780.6:c.1192T>G ENSP00000369106.2:p.Phe398Val
ENST00000566128.1:c.1177T>G ENSP00000456276.1:p.Phe393Val
NM_000078.2:c.1372T>G NP_000069.2:p.Phe458Val
NM_001286085.1:c.1192T>G NP_001273014.1:p.Phe398Val
NM_000078.3:c.1372T>G MANE Select NP_000069.2:p.Phe458Val
NM_001286085.2:c.1192T>G NP_001273014.1:p.Phe398Val