Canonical Allele Identifier: CA2224395607

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968726_56968731delinsCTTCTT , CM000678.2:g.56968726_56968731delinsCTTCTT	GRCh38
NC_000016.9:g.57002638_57002643delinsCTTCTT , CM000678.1:g.57002638_57002643delinsCTTCTT	GRCh37
NC_000016.8:g.55560139_55560144delinsCTTCTT	NCBI36
NG_008952.1:g.11804_11809delinsCTTCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-660_234-655delinsCTTCTT MANE Select	ENSP00000200676.3:n.234-660_234-655delins...
ENST00000200676.7:c.234-660_234-655delinsCTTCTT	ENSP00000200676.3:n.234-660_234-655delins...
ENST00000379780.6:c.234-660_234-655delinsCTTCTT	ENSP00000369106.2:n.234-660_234-655delins...
ENST00000566128.1:c.39-660_39-655delinsCTTCTT	ENSP00000456276.1:n.39-660_39-655delinsCT...
ENST00000569082.1:n.232-660_232-655delinsCTTCTT
NM_000078.2:c.234-660_234-655delinsCTTCTT	NP_000069.2:n.234-660_234-655delinsCTTCTT...
NM_001286085.1:c.234-660_234-655delinsCTTCTT	NP_001273014.1:n.234-660_234-655delinsCTT...
XM_006721124.2:c.234-660_234-655delinsCTTCTT	XP_006721187.1:n.234-660_234-655delinsCTT...
XM_006721124.3:c.234-660_234-655delinsCTTCTT	XP_006721187.1:n.234-660_234-655delinsCTT...
NM_000078.3:c.234-660_234-655delinsCTTCTT MANE Select	NP_000069.2:n.234-660_234-655delinsCTTCTT...
NM_001286085.2:c.234-660_234-655delinsCTTCTT	NP_001273014.1:n.234-660_234-655delinsCTT...