Canonical Allele Identifier: CA2224400100

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56975134C= , CM000678.2:g.56975134C=	GRCh38
NC_000016.9:g.57009046C= , CM000678.1:g.57009046C=	GRCh37
NC_000016.8:g.55566547C=	NCBI36
NG_008952.1:g.18212C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.964C= MANE Select	ENSP00000200676.3:p.Gln322=
ENST00000200676.7:c.964C=	ENSP00000200676.3:p.Gln322=
ENST00000379780.6:c.784C=	ENSP00000369106.2:p.Gln262=
ENST00000566128.1:c.769C=	ENSP00000456276.1:p.Gln257=
NM_000078.2:c.964C=	NP_000069.2:p.Gln322=
NM_001286085.1:c.784C=	NP_001273014.1:p.Gln262=
NM_000078.3:c.964C= MANE Select	NP_000069.2:p.Gln322=
NM_001286085.2:c.784C=	NP_001273014.1:p.Gln262=