Canonical Allele Identifier: CA495622365

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017239G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983327G>T , CM000678.2:g.56983327G>T	GRCh38
NC_000016.9:g.57017239G>T , CM000678.1:g.57017239G>T	GRCh37
NC_000016.8:g.55574740G>T	NCBI36
NG_008952.1:g.26405G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1323G>T MANE Select	ENSP00000200676.3:p.Arg441=
ENST00000650358.1:n.1721G>T
ENST00000200676.7:c.1323G>T	ENSP00000200676.3:p.Arg441=
ENST00000379780.6:c.1143G>T	ENSP00000369106.2:p.Arg381=
ENST00000566128.1:c.1128G>T	ENSP00000456276.1:p.Arg376=
NM_000078.2:c.1323G>T	NP_000069.2:p.Arg441=
NM_001286085.1:c.1143G>T	NP_001273014.1:p.Arg381=
NM_000078.3:c.1323G>T MANE Select	NP_000069.2:p.Arg441=
NM_001286085.2:c.1143G>T	NP_001273014.1:p.Arg381=