Canonical Allele Identifier: CA396008021

Gene: CETP

Linked Data

• COSMIC: COSM3672286
• MyVariant Identifiers: chr16:g.57017243G>T (hg19) ; chr16:g.56983331G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983331G>T , CM000678.2:g.56983331G>T	GRCh38
NC_000016.9:g.57017243G>T , CM000678.1:g.57017243G>T	GRCh37
NC_000016.8:g.55574744G>T	NCBI36
NG_008952.1:g.26409G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1327G>T MANE Select	ENSP00000200676.3:p.Glu443Ter
ENST00000650358.1:n.1725G>T
ENST00000200676.7:c.1327G>T	ENSP00000200676.3:p.Glu443Ter
ENST00000379780.6:c.1147G>T	ENSP00000369106.2:p.Glu383Ter
ENST00000566128.1:c.1132G>T	ENSP00000456276.1:p.Glu378Ter
NM_000078.2:c.1327G>T	NP_000069.2:p.Glu443Ter
NM_001286085.1:c.1147G>T	NP_001273014.1:p.Glu383Ter
NM_000078.3:c.1327G>T MANE Select	NP_000069.2:p.Glu443Ter
NM_001286085.2:c.1147G>T	NP_001273014.1:p.Glu383Ter