Canonical Allele Identifier: CA622341847

Gene: CETP

Linked Data

• dbSNP Id: rs1317189271
• gnomAD v2: 16-57005480-T-TCA
• gnomAD v3: 16-56971568-T-TCA
• gnomAD v4: 16-56971568-T-TCA
• MyVariant Identifiers: chr16:g.57005480_57005481insCA (hg19) ; chr16:g.56971568_56971569insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971571_56971572dup , CM000678.2:g.56971571_56971572dup	GRCh38
NC_000016.9:g.57005483_57005484dup , CM000678.1:g.57005483_57005484dup	GRCh37
NC_000016.8:g.55562984_55562985dup	NCBI36
NG_008952.1:g.14649_14650dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.658+190_658+191dup MANE Select	ENSP00000200676.3:n.658+190_658+191dup
ENST00000200676.7:c.658+190_658+191dup	ENSP00000200676.3:n.658+190_658+191dup
ENST00000379780.6:c.658+190_658+191dup	ENSP00000369106.2:n.658+190_658+191dup
ENST00000566128.1:c.463+190_463+191dup	ENSP00000456276.1:n.463+190_463+191dup
ENST00000569082.1:n.760+190_760+191dup
NM_000078.2:c.658+190_658+191dup	NP_000069.2:n.658+190_658+191dup
NM_001286085.1:c.658+190_658+191dup	NP_001273014.1:n.658+190_658+191dup
XM_006721124.2:c.658+190_658+191dup	XP_006721187.1:n.658+190_658+191dup
XM_006721124.3:c.658+190_658+191dup	XP_006721187.1:n.658+190_658+191dup
NM_000078.3:c.658+190_658+191dup MANE Select	NP_000069.2:n.658+190_658+191dup
NM_001286085.2:c.658+190_658+191dup	NP_001273014.1:n.658+190_658+191dup