Canonical Allele Identifier: CA2224396333

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56978387G= , CM000678.2:g.56978387G=	GRCh38
NC_000016.9:g.57012299G= , CM000678.1:g.57012299G=	GRCh37
NC_000016.8:g.55569800G=	NCBI36
NG_008952.1:g.21465G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1146+132G= MANE Select	ENSP00000200676.3:n.1146+132G=
ENST00000650358.1:n.1544+132G=
ENST00000200676.7:c.1146+132G=	ENSP00000200676.3:n.1146+132G=
ENST00000379780.6:c.966+132G=	ENSP00000369106.2:n.966+132G=
ENST00000566128.1:c.951+132G=	ENSP00000456276.1:n.951+132G=
NM_000078.2:c.1146+132G=	NP_000069.2:n.1146+132G=
NM_001286085.1:c.966+132G=	NP_001273014.1:n.966+132G=
NM_000078.3:c.1146+132G= MANE Select	NP_000069.2:n.1146+132G=
NM_001286085.2:c.966+132G=	NP_001273014.1:n.966+132G=