Canonical Allele Identifier: CA2633384949

Gene: CETP

Linked Data

• gnomAD v4: 16-56963222-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56963222G>A , CM000678.2:g.56963222G>A	GRCh38
NC_000016.9:g.56997134G>A , CM000678.1:g.56997134G>A	GRCh37
NC_000016.8:g.55554635G>A	NCBI36
NG_008952.1:g.6300G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.233+98G>A MANE Select	ENSP00000200676.3:n.233+98G>A
ENST00000200676.7:c.233+98G>A	ENSP00000200676.3:n.233+98G>A
ENST00000379780.6:c.233+98G>A	ENSP00000369106.2:n.233+98G>A
ENST00000566128.1:c.38+98G>A	ENSP00000456276.1:n.38+98G>A
ENST00000569082.1:n.231+98G>A
NM_000078.2:c.233+98G>A	NP_000069.2:n.233+98G>A
NM_001286085.1:c.233+98G>A	NP_001273014.1:n.233+98G>A
XM_006721124.2:c.233+98G>A	XP_006721187.1:n.233+98G>A
XM_006721124.3:c.233+98G>A	XP_006721187.1:n.233+98G>A
NM_000078.3:c.233+98G>A MANE Select	NP_000069.2:n.233+98G>A
NM_001286085.2:c.233+98G>A	NP_001273014.1:n.233+98G>A