Canonical Allele Identifier: CA2505238665

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968742_56968743insC , CM000678.2:g.56968742_56968743insC	GRCh38
NC_000016.9:g.57002654_57002655insC , CM000678.1:g.57002654_57002655insC	GRCh37
NC_000016.8:g.55560155_55560156insC	NCBI36
NG_008952.1:g.11820_11821insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-644_234-643insC MANE Select	ENSP00000200676.3:n.234-644_234-643insC
ENST00000200676.7:c.234-644_234-643insC	ENSP00000200676.3:n.234-644_234-643insC
ENST00000379780.6:c.234-644_234-643insC	ENSP00000369106.2:n.234-644_234-643insC
ENST00000566128.1:c.39-644_39-643insC	ENSP00000456276.1:n.39-644_39-643insC
ENST00000569082.1:n.232-644_232-643insC
NM_000078.2:c.234-644_234-643insC	NP_000069.2:n.234-644_234-643insC
NM_001286085.1:c.234-644_234-643insC	NP_001273014.1:n.234-644_234-643insC
XM_006721124.2:c.234-644_234-643insC	XP_006721187.1:n.234-644_234-643insC
XM_006721124.3:c.234-644_234-643insC	XP_006721187.1:n.234-644_234-643insC
NM_000078.3:c.234-644_234-643insC MANE Select	NP_000069.2:n.234-644_234-643insC
NM_001286085.2:c.234-644_234-643insC	NP_001273014.1:n.234-644_234-643insC