Canonical Allele Identifier: CA977671256

Gene: CETP

Linked Data

• gnomAD v3: 16-56968817-GTTT-G
• gnomAD v4: 16-56968817-GTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968820_56968822del , CM000678.2:g.56968820_56968822del	GRCh38
NC_000016.9:g.57002732_57002734del , CM000678.1:g.57002732_57002734del	GRCh37
NC_000016.8:g.55560233_55560235del	NCBI36
NG_008952.1:g.11898_11900del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-566_234-564del MANE Select	ENSP00000200676.3:n.234-566_234-564del
ENST00000200676.7:c.234-566_234-564del	ENSP00000200676.3:n.234-566_234-564del
ENST00000379780.6:c.234-566_234-564del	ENSP00000369106.2:n.234-566_234-564del
ENST00000566128.1:c.39-566_39-564del	ENSP00000456276.1:n.39-566_39-564del
ENST00000569082.1:n.232-566_232-564del
NM_000078.2:c.234-566_234-564del	NP_000069.2:n.234-566_234-564del
NM_001286085.1:c.234-566_234-564del	NP_001273014.1:n.234-566_234-564del
XM_006721124.2:c.234-566_234-564del	XP_006721187.1:n.234-566_234-564del
XM_006721124.3:c.234-566_234-564del	XP_006721187.1:n.234-566_234-564del
NM_000078.3:c.234-566_234-564del MANE Select	NP_000069.2:n.234-566_234-564del
NM_001286085.2:c.234-566_234-564del	NP_001273014.1:n.234-566_234-564del