Canonical Allele Identifier: CA977671030

Gene: CETP

Linked Data

• gnomAD v3: 16-56968729-C-CTTTTTTTTTTTTTTT
• gnomAD v4: 16-56968729-C-CTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968730_56968744dup , CM000678.2:g.56968730_56968744dup	GRCh38
NC_000016.9:g.57002642_57002656dup , CM000678.1:g.57002642_57002656dup	GRCh37
NC_000016.8:g.55560143_55560157dup	NCBI36
NG_008952.1:g.11808_11822dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-656_234-642dup MANE Select	ENSP00000200676.3:n.234-656_234-642dup
ENST00000200676.7:c.234-656_234-642dup	ENSP00000200676.3:n.234-656_234-642dup
ENST00000379780.6:c.234-656_234-642dup	ENSP00000369106.2:n.234-656_234-642dup
ENST00000566128.1:c.39-656_39-642dup	ENSP00000456276.1:n.39-656_39-642dup
ENST00000569082.1:n.232-656_232-642dup
NM_000078.2:c.234-656_234-642dup	NP_000069.2:n.234-656_234-642dup
NM_001286085.1:c.234-656_234-642dup	NP_001273014.1:n.234-656_234-642dup
XM_006721124.2:c.234-656_234-642dup	XP_006721187.1:n.234-656_234-642dup
XM_006721124.3:c.234-656_234-642dup	XP_006721187.1:n.234-656_234-642dup
NM_000078.3:c.234-656_234-642dup MANE Select	NP_000069.2:n.234-656_234-642dup
NM_001286085.2:c.234-656_234-642dup	NP_001273014.1:n.234-656_234-642dup