Canonical Allele Identifier: CA2224395690

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968887_56968888delinsCT , CM000678.2:g.56968887_56968888delinsCT	GRCh38
NC_000016.9:g.57002799_57002800delinsCT , CM000678.1:g.57002799_57002800delinsCT	GRCh37
NC_000016.8:g.55560300_55560301delinsCT	NCBI36
NG_008952.1:g.11965_11966delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-499_234-498delinsCT MANE Select	ENSP00000200676.3:n.234-499_234-498delins...
ENST00000200676.7:c.234-499_234-498delinsCT	ENSP00000200676.3:n.234-499_234-498delins...
ENST00000379780.6:c.234-499_234-498delinsCT	ENSP00000369106.2:n.234-499_234-498delins...
ENST00000566128.1:c.39-499_39-498delinsCT	ENSP00000456276.1:n.39-499_39-498delinsCT...
ENST00000569082.1:n.232-499_232-498delinsCT
NM_000078.2:c.234-499_234-498delinsCT	NP_000069.2:n.234-499_234-498delinsCT
NM_001286085.1:c.234-499_234-498delinsCT	NP_001273014.1:n.234-499_234-498delinsCT
XM_006721124.2:c.234-499_234-498delinsCT	XP_006721187.1:n.234-499_234-498delinsCT
XM_006721124.3:c.234-499_234-498delinsCT	XP_006721187.1:n.234-499_234-498delinsCT
NM_000078.3:c.234-499_234-498delinsCT MANE Select	NP_000069.2:n.234-499_234-498delinsCT
NM_001286085.2:c.234-499_234-498delinsCT	NP_001273014.1:n.234-499_234-498delinsCT