Canonical Allele Identifier: CA977671065

Gene: CETP

Linked Data

• gnomAD v3: 16-56968744-TGCCAGTCTAGCTAAAGGTTTGTTGA-T
• gnomAD v4: 16-56968744-TGCCAGTCTAGCTAAAGGTTTGTTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968745_56968769del , CM000678.2:g.56968745_56968769del	GRCh38
NC_000016.9:g.57002657_57002681del , CM000678.1:g.57002657_57002681del	GRCh37
NC_000016.8:g.55560158_55560182del	NCBI36
NG_008952.1:g.11823_11847del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-641_234-617del MANE Select	ENSP00000200676.3:n.234-641_234-617del
ENST00000200676.7:c.234-641_234-617del	ENSP00000200676.3:n.234-641_234-617del
ENST00000379780.6:c.234-641_234-617del	ENSP00000369106.2:n.234-641_234-617del
ENST00000566128.1:c.39-641_39-617del	ENSP00000456276.1:n.39-641_39-617del
ENST00000569082.1:n.232-641_232-617del
NM_000078.2:c.234-641_234-617del	NP_000069.2:n.234-641_234-617del
NM_001286085.1:c.234-641_234-617del	NP_001273014.1:n.234-641_234-617del
XM_006721124.2:c.234-641_234-617del	XP_006721187.1:n.234-641_234-617del
XM_006721124.3:c.234-641_234-617del	XP_006721187.1:n.234-641_234-617del
NM_000078.3:c.234-641_234-617del MANE Select	NP_000069.2:n.234-641_234-617del
NM_001286085.2:c.234-641_234-617del	NP_001273014.1:n.234-641_234-617del