Canonical Allele Identifier: CA8070898

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56969625A>T , CM000678.2:g.56969625A>T	GRCh38
NC_000016.9:g.57003537A>T , CM000678.1:g.57003537A>T	GRCh37
NC_000016.8:g.55561038A>T	NCBI36
NG_008952.1:g.12703A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000078.3:c.383A>T MANE Select	NP_000069.2:p.Gln128Leu
ENST00000200676.8:c.383A>T MANE Select	ENSP00000200676.3:p.Gln128Leu
NM_000078.2:c.383A>T	NP_000069.2:p.Gln128Leu
NM_001286085.1:c.383A>T	NP_001273014.1:p.Gln128Leu
NM_001286085.2:c.383A>T	NP_001273014.1:p.Gln128Leu
ENST00000200676.7:c.383A>T	ENSP00000200676.3:p.Gln128Leu
ENST00000379780.6:c.383A>T	ENSP00000369106.2:p.Gln128Leu
ENST00000566128.1:c.188A>T	ENSP00000456276.1:p.Gln63Leu
ENST00000569082.1:n.381A>T
XM_006721124.2:c.383A>T	XP_006721187.1:p.Gln128Leu
XM_006721124.3:c.383A>T	XP_006721187.1:p.Gln128Leu