Canonical Allele Identifier: CA2839908601

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983349dup , CM000678.2:g.56983349dup	GRCh38
NC_000016.9:g.57017261dup , CM000678.1:g.57017261dup	GRCh37
NC_000016.8:g.55574762dup	NCBI36
NG_008952.1:g.26427dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1345dup MANE Select	ENSP00000200676.3:p.Leu449ProfsTer16
ENST00000650358.1:n.1743dup
ENST00000200676.7:c.1345dup	ENSP00000200676.3:p.Leu449ProfsTer16
ENST00000379780.6:c.1165dup	ENSP00000369106.2:p.Leu389ProfsTer16
ENST00000566128.1:c.1150dup	ENSP00000456276.1:p.Leu384ProfsTer16
NM_000078.2:c.1345dup	NP_000069.2:p.Leu449ProfsTer16
NM_001286085.1:c.1165dup	NP_001273014.1:p.Leu389ProfsTer16
NM_000078.3:c.1345dup MANE Select	NP_000069.2:p.Leu449ProfsTer16
NM_001286085.2:c.1165dup	NP_001273014.1:p.Leu389ProfsTer16