Canonical Allele Identifier: CA2224396337

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56978390C= , CM000678.2:g.56978390C=	GRCh38
NC_000016.9:g.57012302C= , CM000678.1:g.57012302C=	GRCh37
NC_000016.8:g.55569803C=	NCBI36
NG_008952.1:g.21468C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1146+135C= MANE Select	ENSP00000200676.3:n.1146+135C=
ENST00000650358.1:n.1544+135C=
ENST00000200676.7:c.1146+135C=	ENSP00000200676.3:n.1146+135C=
ENST00000379780.6:c.966+135C=	ENSP00000369106.2:n.966+135C=
ENST00000566128.1:c.951+135C=	ENSP00000456276.1:n.951+135C=
NM_000078.2:c.1146+135C=	NP_000069.2:n.1146+135C=
NM_001286085.1:c.966+135C=	NP_001273014.1:n.966+135C=
NM_000078.3:c.1146+135C= MANE Select	NP_000069.2:n.1146+135C=
NM_001286085.2:c.966+135C=	NP_001273014.1:n.966+135C=