Canonical Allele Identifier: CA2633387112

Gene: CETP

Linked Data

• gnomAD v4: 16-56982015-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56982015C>G , CM000678.2:g.56982015C>G	GRCh38
NC_000016.9:g.57015927C>G , CM000678.1:g.57015927C>G	GRCh37
NC_000016.8:g.55573428C>G	NCBI36
NG_008952.1:g.25093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1249-150C>G MANE Select	ENSP00000200676.3:n.1249-150C>G
ENST00000650358.1:n.1647-150C>G
ENST00000200676.7:c.1249-150C>G	ENSP00000200676.3:n.1249-150C>G
ENST00000379780.6:c.1069-150C>G	ENSP00000369106.2:n.1069-150C>G
ENST00000566128.1:c.1054-150C>G	ENSP00000456276.1:n.1054-150C>G
NM_000078.2:c.1249-150C>G	NP_000069.2:n.1249-150C>G
NM_001286085.1:c.1069-150C>G	NP_001273014.1:n.1069-150C>G
NM_000078.3:c.1249-150C>G MANE Select	NP_000069.2:n.1249-150C>G
NM_001286085.2:c.1069-150C>G	NP_001273014.1:n.1069-150C>G