Canonical Allele Identifier: CA396008186

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017277G>T (hg19) ; chr16:g.56983365G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983365G>T , CM000678.2:g.56983365G>T	GRCh38
NC_000016.9:g.57017277G>T , CM000678.1:g.57017277G>T	GRCh37
NC_000016.8:g.55574778G>T	NCBI36
NG_008952.1:g.26443G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1361G>T MANE Select	ENSP00000200676.3:p.Gly454Val
ENST00000650358.1:n.1759G>T
ENST00000200676.7:c.1361G>T	ENSP00000200676.3:p.Gly454Val
ENST00000379780.6:c.1181G>T	ENSP00000369106.2:p.Gly394Val
ENST00000566128.1:c.1166G>T	ENSP00000456276.1:p.Gly389Val
NM_000078.2:c.1361G>T	NP_000069.2:p.Gly454Val
NM_001286085.1:c.1181G>T	NP_001273014.1:p.Gly394Val
NM_000078.3:c.1361G>T MANE Select	NP_000069.2:p.Gly454Val
NM_001286085.2:c.1181G>T	NP_001273014.1:p.Gly394Val