Canonical Allele Identifier: CA8071359

Gene: CETP

Linked Data

• dbSNP Id: rs753962259
• ExAC: 16:57017239 G / A
• MyVariant Identifiers: chr16:g.57017239G>A (hg19) ; chr16:g.56983327G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983327G>A , CM000678.2:g.56983327G>A	GRCh38
NC_000016.9:g.57017239G>A , CM000678.1:g.57017239G>A	GRCh37
NC_000016.8:g.55574740G>A	NCBI36
NG_008952.1:g.26405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1323G>A MANE Select	ENSP00000200676.3:p.Arg441=
ENST00000650358.1:n.1721G>A
ENST00000200676.7:c.1323G>A	ENSP00000200676.3:p.Arg441=
ENST00000379780.6:c.1143G>A	ENSP00000369106.2:p.Arg381=
ENST00000566128.1:c.1128G>A	ENSP00000456276.1:p.Arg376=
NM_000078.2:c.1323G>A	NP_000069.2:p.Arg441=
NM_001286085.1:c.1143G>A	NP_001273014.1:p.Arg381=
NM_000078.3:c.1323G>A MANE Select	NP_000069.2:p.Arg441=
NM_001286085.2:c.1143G>A	NP_001273014.1:p.Arg381=