Canonical Allele Identifier: CA396008163

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017272C>A (hg19) ; chr16:g.56983360C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983360C>A , CM000678.2:g.56983360C>A	GRCh38
NC_000016.9:g.57017272C>A , CM000678.1:g.57017272C>A	GRCh37
NC_000016.8:g.55574773C>A	NCBI36
NG_008952.1:g.26438C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1356C>A MANE Select	ENSP00000200676.3:p.Ser452Arg
ENST00000650358.1:n.1754C>A
ENST00000200676.7:c.1356C>A	ENSP00000200676.3:p.Ser452Arg
ENST00000379780.6:c.1176C>A	ENSP00000369106.2:p.Ser392Arg
ENST00000566128.1:c.1161C>A	ENSP00000456276.1:p.Ser387Arg
NM_000078.2:c.1356C>A	NP_000069.2:p.Ser452Arg
NM_001286085.1:c.1176C>A	NP_001273014.1:p.Ser392Arg
NM_000078.3:c.1356C>A MANE Select	NP_000069.2:p.Ser452Arg
NM_001286085.2:c.1176C>A	NP_001273014.1:p.Ser392Arg