Canonical Allele Identifier: CA396008331

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017309A>C (hg19) ; chr16:g.56983397A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983397A>C , CM000678.2:g.56983397A>C	GRCh38
NC_000016.9:g.57017309A>C , CM000678.1:g.57017309A>C	GRCh37
NC_000016.8:g.55574810A>C	NCBI36
NG_008952.1:g.26475A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1393A>C MANE Select	ENSP00000200676.3:p.Ile465Leu
ENST00000200676.7:c.1393A>C	ENSP00000200676.3:p.Ile465Leu
ENST00000379780.6:c.1213A>C	ENSP00000369106.2:p.Ile405Leu
ENST00000566128.1:c.1198A>C	ENSP00000456276.1:p.Ile400Leu
NM_000078.2:c.1393A>C	NP_000069.2:p.Ile465Leu
NM_001286085.1:c.1213A>C	NP_001273014.1:p.Ile405Leu
NM_000078.3:c.1393A>C MANE Select	NP_000069.2:p.Ile465Leu
NM_001286085.2:c.1213A>C	NP_001273014.1:p.Ile405Leu