Canonical Allele Identifier: CA2224402559

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983379G= , CM000678.2:g.56983379G=	GRCh38
NC_000016.9:g.57017291G= , CM000678.1:g.57017291G=	GRCh37
NC_000016.8:g.55574792G=	NCBI36
NG_008952.1:g.26457G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1375G= MANE Select	ENSP00000200676.3:p.Asp459=
ENST00000650358.1:n.1773G=
ENST00000200676.7:c.1375G=	ENSP00000200676.3:p.Asp459=
ENST00000379780.6:c.1195G=	ENSP00000369106.2:p.Asp399=
ENST00000566128.1:c.1180G=	ENSP00000456276.1:p.Asp394=
NM_000078.2:c.1375G=	NP_000069.2:p.Asp459=
NM_001286085.1:c.1195G=	NP_001273014.1:p.Asp399=
NM_000078.3:c.1375G= MANE Select	NP_000069.2:p.Asp459=
NM_001286085.2:c.1195G=	NP_001273014.1:p.Asp399=