Canonical Allele Identifier: CA2633385976

Gene: CETP

Linked Data

• gnomAD v4: 16-56971399-T-TTCTGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971399_56971400insTCTGAG , CM000678.2:g.56971399_56971400insTCTGAG	GRCh38
NC_000016.9:g.57005311_57005312insTCTGAG , CM000678.1:g.57005311_57005312insTCTGAG	GRCh37
NC_000016.8:g.55562812_55562813insTCTGAG	NCBI36
NG_008952.1:g.14477_14478insTCTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.658+18_658+19insTCTGAG MANE Select	ENSP00000200676.3:n.658+18_658+19insTCTGAG
ENST00000200676.7:c.658+18_658+19insTCTGAG	ENSP00000200676.3:n.658+18_658+19insTCTGAG
ENST00000379780.6:c.658+18_658+19insTCTGAG	ENSP00000369106.2:n.658+18_658+19insTCTGAG
ENST00000566128.1:c.463+18_463+19insTCTGAG	ENSP00000456276.1:n.463+18_463+19insTCTGAG
ENST00000569082.1:n.760+18_760+19insTCTGAG
NM_000078.2:c.658+18_658+19insTCTGAG	NP_000069.2:n.658+18_658+19insTCTGAG
NM_001286085.1:c.658+18_658+19insTCTGAG	NP_001273014.1:n.658+18_658+19insTCTGAG
XM_006721124.2:c.658+18_658+19insTCTGAG	XP_006721187.1:n.658+18_658+19insTCTGAG
XM_006721124.3:c.658+18_658+19insTCTGAG	XP_006721187.1:n.658+18_658+19insTCTGAG
NM_000078.3:c.658+18_658+19insTCTGAG MANE Select	NP_000069.2:n.658+18_658+19insTCTGAG
NM_001286085.2:c.658+18_658+19insTCTGAG	NP_001273014.1:n.658+18_658+19insTCTGAG