Canonical Allele Identifier: CA977671060

Gene: CETP

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968746_56968749del , CM000678.2:g.56968746_56968749del	GRCh38
NC_000016.9:g.57002658_57002661del , CM000678.1:g.57002658_57002661del	GRCh37
NC_000016.8:g.55560159_55560162del	NCBI36
NG_008952.1:g.11824_11827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.234-640_234-637del MANE Select	ENSP00000200676.3:n.234-640_234-637del
ENST00000200676.7:c.234-640_234-637del	ENSP00000200676.3:n.234-640_234-637del
ENST00000379780.6:c.234-640_234-637del	ENSP00000369106.2:n.234-640_234-637del
ENST00000566128.1:c.39-640_39-637del	ENSP00000456276.1:n.39-640_39-637del
ENST00000569082.1:n.232-640_232-637del
NM_000078.2:c.234-640_234-637del	NP_000069.2:n.234-640_234-637del
NM_001286085.1:c.234-640_234-637del	NP_001273014.1:n.234-640_234-637del
XM_006721124.2:c.234-640_234-637del	XP_006721187.1:n.234-640_234-637del
XM_006721124.3:c.234-640_234-637del	XP_006721187.1:n.234-640_234-637del
NM_000078.3:c.234-640_234-637del MANE Select	NP_000069.2:n.234-640_234-637del
NM_001286085.2:c.234-640_234-637del	NP_001273014.1:n.234-640_234-637del