Canonical Allele Identifier: CA622341851

Gene: CETP

Linked Data

• dbSNP Id: rs1471807258
• gnomAD v2: 16-57005530-TGATTAAGTCCAAGAGGACTCCAA-T
• gnomAD v3: 16-56971618-TGATTAAGTCCAAGAGGACTCCAA-T
• gnomAD v4: 16-56971618-TGATTAAGTCCAAGAGGACTCCAA-T
• MyVariant Identifiers: chr16:g.57005531_57005553del (hg19) ; chr16:g.56971619_56971641del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971623_56971645del , CM000678.2:g.56971623_56971645del	GRCh38
NC_000016.9:g.57005535_57005557del , CM000678.1:g.57005535_57005557del	GRCh37
NC_000016.8:g.55563036_55563058del	NCBI36
NG_008952.1:g.14701_14723del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.658+242_658+264del MANE Select	ENSP00000200676.3:n.658+242_658+264del
ENST00000200676.7:c.658+242_658+264del	ENSP00000200676.3:n.658+242_658+264del
ENST00000379780.6:c.658+242_658+264del	ENSP00000369106.2:n.658+242_658+264del
ENST00000566128.1:c.463+242_463+264del	ENSP00000456276.1:n.463+242_463+264del
ENST00000569082.1:n.760+242_760+264del
NM_000078.2:c.658+242_658+264del	NP_000069.2:n.658+242_658+264del
NM_001286085.1:c.658+242_658+264del	NP_001273014.1:n.658+242_658+264del
XM_006721124.2:c.658+242_658+264del	XP_006721187.1:n.658+242_658+264del
XM_006721124.3:c.658+242_658+264del	XP_006721187.1:n.658+242_658+264del
NM_000078.3:c.658+242_658+264del MANE Select	NP_000069.2:n.658+242_658+264del
NM_001286085.2:c.658+242_658+264del	NP_001273014.1:n.658+242_658+264del