Canonical Allele Identifier: CA396008029

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017244A>T (hg19) ; chr16:g.56983332A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1328A>T MANE Select	ENSP00000200676.3:p.Glu443Val
ENST00000650358.1:n.1726A>T
ENST00000200676.7:c.1328A>T	ENSP00000200676.3:p.Glu443Val
ENST00000379780.6:c.1148A>T	ENSP00000369106.2:p.Glu383Val
ENST00000566128.1:c.1133A>T	ENSP00000456276.1:p.Glu378Val
NM_000078.2:c.1328A>T	NP_000069.2:p.Glu443Val
NM_001286085.1:c.1148A>T	NP_001273014.1:p.Glu383Val
NM_000078.3:c.1328A>T MANE Select	NP_000069.2:p.Glu443Val
NM_001286085.2:c.1148A>T	NP_001273014.1:p.Glu383Val