Canonical Allele Identifier: CA2224392930

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56963288A= , CM000678.2:g.56963288A=	GRCh38
NC_000016.9:g.56997200A= , CM000678.1:g.56997200A=	GRCh37
NC_000016.8:g.55554701A=	NCBI36
NG_008952.1:g.6366A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.233+164A= MANE Select	ENSP00000200676.3:n.233+164A=
ENST00000200676.7:c.233+164A=	ENSP00000200676.3:n.233+164A=
ENST00000379780.6:c.233+164A=	ENSP00000369106.2:n.233+164A=
ENST00000566128.1:c.38+164A=	ENSP00000456276.1:n.38+164A=
ENST00000569082.1:n.231+164A=
NM_000078.2:c.233+164A=	NP_000069.2:n.233+164A=
NM_001286085.1:c.233+164A=	NP_001273014.1:n.233+164A=
XM_006721124.2:c.233+164A=	XP_006721187.1:n.233+164A=
XM_006721124.3:c.233+164A=	XP_006721187.1:n.233+164A=
NM_000078.3:c.233+164A= MANE Select	NP_000069.2:n.233+164A=
NM_001286085.2:c.233+164A=	NP_001273014.1:n.233+164A=