Canonical Allele Identifier: CA2224402583

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983439_56983441delinsCCT , CM000678.2:g.56983439_56983441delinsCCT	GRCh38
NC_000016.9:g.57017351_57017353delinsCCT , CM000678.1:g.57017351_57017353delinsCCT	GRCh37
NC_000016.8:g.55574852_55574854delinsCCT	NCBI36
NG_008952.1:g.26517_26519delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1407+28_1407+30delinsCCT MANE Select	ENSP00000200676.3:n.1407+28_1407+30delinsCCT
ENST00000200676.7:c.1407+28_1407+30delinsCCT	ENSP00000200676.3:n.1407+28_1407+30delinsCCT
ENST00000379780.6:c.1227+28_1227+30delinsCCT	ENSP00000369106.2:n.1227+28_1227+30delinsCCT
ENST00000566128.1:c.1212+28_1212+30delinsCCT	ENSP00000456276.1:n.1212+28_1212+30delinsCCT
NM_000078.2:c.1407+28_1407+30delinsCCT	NP_000069.2:n.1407+28_1407+30delinsCCT
NM_001286085.1:c.1227+28_1227+30delinsCCT	NP_001273014.1:n.1227+28_1227+30delinsCCT
NM_000078.3:c.1407+28_1407+30delinsCCT MANE Select	NP_000069.2:n.1407+28_1407+30delinsCCT
NM_001286085.2:c.1227+28_1227+30delinsCCT	NP_001273014.1:n.1227+28_1227+30delinsCCT