Canonical Allele Identifier: CA396004125

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57009037A>G (hg19) ; chr16:g.56975125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56975125A>G , CM000678.2:g.56975125A>G	GRCh38
NC_000016.9:g.57009037A>G , CM000678.1:g.57009037A>G	GRCh37
NC_000016.8:g.55566538A>G	NCBI36
NG_008952.1:g.18203A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.955A>G MANE Select	ENSP00000200676.3:p.Asn319Asp
ENST00000200676.7:c.955A>G	ENSP00000200676.3:p.Asn319Asp
ENST00000379780.6:c.775A>G	ENSP00000369106.2:p.Asn259Asp
ENST00000566128.1:c.760A>G	ENSP00000456276.1:p.Asn254Asp
NM_000078.2:c.955A>G	NP_000069.2:p.Asn319Asp
NM_001286085.1:c.775A>G	NP_001273014.1:p.Asn259Asp
NM_000078.3:c.955A>G MANE Select	NP_000069.2:p.Asn319Asp
NM_001286085.2:c.775A>G	NP_001273014.1:p.Asn259Asp