Canonical Allele Identifier: CA2224398353

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971502G= , CM000678.2:g.56971502G=	GRCh38
NC_000016.9:g.57005414G= , CM000678.1:g.57005414G=	GRCh37
NC_000016.8:g.55562915G=	NCBI36
NG_008952.1:g.14580G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.658+121G= MANE Select	ENSP00000200676.3:n.658+121G=
ENST00000200676.7:c.658+121G=	ENSP00000200676.3:n.658+121G=
ENST00000379780.6:c.658+121G=	ENSP00000369106.2:n.658+121G=
ENST00000566128.1:c.463+121G=	ENSP00000456276.1:n.463+121G=
ENST00000569082.1:n.760+121G=
NM_000078.2:c.658+121G=	NP_000069.2:n.658+121G=
NM_001286085.1:c.658+121G=	NP_001273014.1:n.658+121G=
XM_006721124.2:c.658+121G=	XP_006721187.1:n.658+121G=
XM_006721124.3:c.658+121G=	XP_006721187.1:n.658+121G=
NM_000078.3:c.658+121G= MANE Select	NP_000069.2:n.658+121G=
NM_001286085.2:c.658+121G=	NP_001273014.1:n.658+121G=