Canonical Allele Identifier: CA2224392910

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56963263G= , CM000678.2:g.56963263G=	GRCh38
NC_000016.9:g.56997175G= , CM000678.1:g.56997175G=	GRCh37
NC_000016.8:g.55554676G=	NCBI36
NG_008952.1:g.6341G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.233+139G= MANE Select	ENSP00000200676.3:n.233+139G=
ENST00000200676.7:c.233+139G=	ENSP00000200676.3:n.233+139G=
ENST00000379780.6:c.233+139G=	ENSP00000369106.2:n.233+139G=
ENST00000566128.1:c.38+139G=	ENSP00000456276.1:n.38+139G=
ENST00000569082.1:n.231+139G=
NM_000078.2:c.233+139G=	NP_000069.2:n.233+139G=
NM_001286085.1:c.233+139G=	NP_001273014.1:n.233+139G=
XM_006721124.2:c.233+139G=	XP_006721187.1:n.233+139G=
XM_006721124.3:c.233+139G=	XP_006721187.1:n.233+139G=
NM_000078.3:c.233+139G= MANE Select	NP_000069.2:n.233+139G=
NM_001286085.2:c.233+139G=	NP_001273014.1:n.233+139G=