Canonical Allele Identifier: CA396008335

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017310T>C (hg19) ; chr16:g.56983398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983398T>C , CM000678.2:g.56983398T>C	GRCh38
NC_000016.9:g.57017310T>C , CM000678.1:g.57017310T>C	GRCh37
NC_000016.8:g.55574811T>C	NCBI36
NG_008952.1:g.26476T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1394T>C MANE Select	ENSP00000200676.3:p.Ile465Thr
ENST00000200676.7:c.1394T>C	ENSP00000200676.3:p.Ile465Thr
ENST00000379780.6:c.1214T>C	ENSP00000369106.2:p.Ile405Thr
ENST00000566128.1:c.1199T>C	ENSP00000456276.1:p.Ile400Thr
NM_000078.2:c.1394T>C	NP_000069.2:p.Ile465Thr
NM_001286085.1:c.1214T>C	NP_001273014.1:p.Ile405Thr
NM_000078.3:c.1394T>C MANE Select	NP_000069.2:p.Ile465Thr
NM_001286085.2:c.1214T>C	NP_001273014.1:p.Ile405Thr