Canonical Allele Identifier: CA396004143

Gene: CETP

Linked Data

• dbSNP Id: rs1209112476
• gnomAD v2: 16-57009045-C-A
• gnomAD v4: 16-56975133-C-A
• MyVariant Identifiers: chr16:g.57009045C>A (hg19) ; chr16:g.56975133C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56975133C>A , CM000678.2:g.56975133C>A	GRCh38
NC_000016.9:g.57009045C>A , CM000678.1:g.57009045C>A	GRCh37
NC_000016.8:g.55566546C>A	NCBI36
NG_008952.1:g.18211C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.963C>A MANE Select	ENSP00000200676.3:p.Asn321Lys
ENST00000200676.7:c.963C>A	ENSP00000200676.3:p.Asn321Lys
ENST00000379780.6:c.783C>A	ENSP00000369106.2:p.Asn261Lys
ENST00000566128.1:c.768C>A	ENSP00000456276.1:p.Asn256Lys
NM_000078.2:c.963C>A	NP_000069.2:p.Asn321Lys
NM_001286085.1:c.783C>A	NP_001273014.1:p.Asn261Lys
NM_000078.3:c.963C>A MANE Select	NP_000069.2:p.Asn321Lys
NM_001286085.2:c.783C>A	NP_001273014.1:p.Asn261Lys