Canonical Allele Identifier: CA722015832

Gene: CETP

Linked Data

• dbSNP Id: rs1243727394
• MyVariant Identifiers: chr16:g.57005528G>C (hg19) ; chr16:g.56971616G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971616G>C , CM000678.2:g.56971616G>C	GRCh38
NC_000016.9:g.57005528G>C , CM000678.1:g.57005528G>C	GRCh37
NC_000016.8:g.55563029G>C	NCBI36
NG_008952.1:g.14694G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.658+235G>C MANE Select	ENSP00000200676.3:n.658+235G>C
ENST00000200676.7:c.658+235G>C	ENSP00000200676.3:n.658+235G>C
ENST00000379780.6:c.658+235G>C	ENSP00000369106.2:n.658+235G>C
ENST00000566128.1:c.463+235G>C	ENSP00000456276.1:n.463+235G>C
ENST00000569082.1:n.760+235G>C
NM_000078.2:c.658+235G>C	NP_000069.2:n.658+235G>C
NM_001286085.1:c.658+235G>C	NP_001273014.1:n.658+235G>C
XM_006721124.2:c.658+235G>C	XP_006721187.1:n.658+235G>C
XM_006721124.3:c.658+235G>C	XP_006721187.1:n.658+235G>C
NM_000078.3:c.658+235G>C MANE Select	NP_000069.2:n.658+235G>C
NM_001286085.2:c.658+235G>C	NP_001273014.1:n.658+235G>C