Canonical Allele Identifier: CA2224392955

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56963354_56963355delinsAG , CM000678.2:g.56963354_56963355delinsAG	GRCh38
NC_000016.9:g.56997266_56997267delinsAG , CM000678.1:g.56997266_56997267delinsAG	GRCh37
NC_000016.8:g.55554767_55554768delinsAG	NCBI36
NG_008952.1:g.6432_6433delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.233+230_233+231delinsAG MANE Select	ENSP00000200676.3:n.233+230_233+231delinsAG
ENST00000200676.7:c.233+230_233+231delinsAG	ENSP00000200676.3:n.233+230_233+231delinsAG
ENST00000379780.6:c.233+230_233+231delinsAG	ENSP00000369106.2:n.233+230_233+231delinsAG
ENST00000566128.1:c.38+230_38+231delinsAG	ENSP00000456276.1:n.38+230_38+231delinsAG
ENST00000569082.1:n.231+230_231+231delinsAG
NM_000078.2:c.233+230_233+231delinsAG	NP_000069.2:n.233+230_233+231delinsAG
NM_001286085.1:c.233+230_233+231delinsAG	NP_001273014.1:n.233+230_233+231delinsAG
XM_006721124.2:c.233+230_233+231delinsAG	XP_006721187.1:n.233+230_233+231delinsAG
XM_006721124.3:c.233+230_233+231delinsAG	XP_006721187.1:n.233+230_233+231delinsAG
NM_000078.3:c.233+230_233+231delinsAG MANE Select	NP_000069.2:n.233+230_233+231delinsAG
NM_001286085.2:c.233+230_233+231delinsAG	NP_001273014.1:n.233+230_233+231delinsAG