Canonical Allele Identifier: CA396008131

Gene: CETP

Linked Data

• gnomAD v4: 16-56983355-A-G
• MyVariant Identifiers: chr16:g.57017267A>G (hg19) ; chr16:g.56983355A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983355A>G , CM000678.2:g.56983355A>G	GRCh38
NC_000016.9:g.57017267A>G , CM000678.1:g.57017267A>G	GRCh37
NC_000016.8:g.55574768A>G	NCBI36
NG_008952.1:g.26433A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1351A>G MANE Select	ENSP00000200676.3:p.Asn451Asp
ENST00000650358.1:n.1749A>G
ENST00000200676.7:c.1351A>G	ENSP00000200676.3:p.Asn451Asp
ENST00000379780.6:c.1171A>G	ENSP00000369106.2:p.Asn391Asp
ENST00000566128.1:c.1156A>G	ENSP00000456276.1:p.Asn386Asp
NM_000078.2:c.1351A>G	NP_000069.2:p.Asn451Asp
NM_001286085.1:c.1171A>G	NP_001273014.1:p.Asn391Asp
NM_000078.3:c.1351A>G MANE Select	NP_000069.2:p.Asn451Asp
NM_001286085.2:c.1171A>G	NP_001273014.1:p.Asn391Asp