Canonical Allele Identifier: CA2224395728

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56969002G= , CM000678.2:g.56969002G=	GRCh38
NC_000016.9:g.57002914G= , CM000678.1:g.57002914G=	GRCh37
NC_000016.8:g.55560415G=	NCBI36
NG_008952.1:g.12080G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-384G= MANE Select	ENSP00000200676.3:n.234-384G=
ENST00000200676.7:c.234-384G=	ENSP00000200676.3:n.234-384G=
ENST00000379780.6:c.234-384G=	ENSP00000369106.2:n.234-384G=
ENST00000566128.1:c.39-384G=	ENSP00000456276.1:n.39-384G=
ENST00000569082.1:n.232-384G=
NM_000078.2:c.234-384G=	NP_000069.2:n.234-384G=
NM_001286085.1:c.234-384G=	NP_001273014.1:n.234-384G=
XM_006721124.2:c.234-384G=	XP_006721187.1:n.234-384G=
XM_006721124.3:c.234-384G=	XP_006721187.1:n.234-384G=
NM_000078.3:c.234-384G= MANE Select	NP_000069.2:n.234-384G=
NM_001286085.2:c.234-384G=	NP_001273014.1:n.234-384G=