Canonical Allele Identifier: CA396008026
Gene: CETP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983332A>C , CM000678.2:g.56983332A>C GRCh38
NC_000016.9:g.57017244A>C , CM000678.1:g.57017244A>C GRCh37
NC_000016.8:g.55574745A>C NCBI36
NG_008952.1:g.26410A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1328A>C MANE Select ENSP00000200676.3:p.Glu443Ala
ENST00000650358.1:n.1726A>C
ENST00000200676.7:c.1328A>C ENSP00000200676.3:p.Glu443Ala
ENST00000379780.6:c.1148A>C ENSP00000369106.2:p.Glu383Ala
ENST00000566128.1:c.1133A>C ENSP00000456276.1:p.Glu378Ala
NM_000078.2:c.1328A>C NP_000069.2:p.Glu443Ala
NM_001286085.1:c.1148A>C NP_001273014.1:p.Glu383Ala
NM_000078.3:c.1328A>C MANE Select NP_000069.2:p.Glu443Ala
NM_001286085.2:c.1148A>C NP_001273014.1:p.Glu383Ala