Canonical Allele Identifier: CA2224402531

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983330C= , CM000678.2:g.56983330C=	GRCh38
NC_000016.9:g.57017242C= , CM000678.1:g.57017242C=	GRCh37
NC_000016.8:g.55574743C=	NCBI36
NG_008952.1:g.26408C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1326C= MANE Select	ENSP00000200676.3:p.Leu442=
ENST00000650358.1:n.1724C=
ENST00000200676.7:c.1326C=	ENSP00000200676.3:p.Leu442=
ENST00000379780.6:c.1146C=	ENSP00000369106.2:p.Leu382=
ENST00000566128.1:c.1131C=	ENSP00000456276.1:p.Leu377=
NM_000078.2:c.1326C=	NP_000069.2:p.Leu442=
NM_001286085.1:c.1146C=	NP_001273014.1:p.Leu382=
NM_000078.3:c.1326C= MANE Select	NP_000069.2:p.Leu442=
NM_001286085.2:c.1146C=	NP_001273014.1:p.Leu382=