Canonical Allele Identifier: CA2843554842

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983338dup , CM000678.2:g.56983338dup	GRCh38
NC_000016.9:g.57017250dup , CM000678.1:g.57017250dup	GRCh37
NC_000016.8:g.55574751dup	NCBI36
NG_008952.1:g.26416dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1334dup MANE Select	ENSP00000200676.3:p.Phe446ValfsTer19
ENST00000650358.1:n.1732dup
ENST00000200676.7:c.1334dup	ENSP00000200676.3:p.Phe446ValfsTer19
ENST00000379780.6:c.1154dup	ENSP00000369106.2:p.Phe386ValfsTer19
ENST00000566128.1:c.1139dup	ENSP00000456276.1:p.Phe381ValfsTer19
NM_000078.2:c.1334dup	NP_000069.2:p.Phe446ValfsTer19
NM_001286085.1:c.1154dup	NP_001273014.1:p.Phe386ValfsTer19
NM_000078.3:c.1334dup MANE Select	NP_000069.2:p.Phe446ValfsTer19
NM_001286085.2:c.1154dup	NP_001273014.1:p.Phe386ValfsTer19