Canonical Allele Identifier: CA2633385984

Gene: CETP

Linked Data

• gnomAD v4: 16-56971405-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971407_56971408del , CM000678.2:g.56971407_56971408del	GRCh38
NC_000016.9:g.57005319_57005320del , CM000678.1:g.57005319_57005320del	GRCh37
NC_000016.8:g.55562820_55562821del	NCBI36
NG_008952.1:g.14485_14486del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.658+26_658+27del MANE Select	ENSP00000200676.3:n.658+26_658+27del
ENST00000200676.7:c.658+26_658+27del	ENSP00000200676.3:n.658+26_658+27del
ENST00000379780.6:c.658+26_658+27del	ENSP00000369106.2:n.658+26_658+27del
ENST00000566128.1:c.463+26_463+27del	ENSP00000456276.1:n.463+26_463+27del
ENST00000569082.1:n.760+26_760+27del
NM_000078.2:c.658+26_658+27del	NP_000069.2:n.658+26_658+27del
NM_001286085.1:c.658+26_658+27del	NP_001273014.1:n.658+26_658+27del
XM_006721124.2:c.658+26_658+27del	XP_006721187.1:n.658+26_658+27del
XM_006721124.3:c.658+26_658+27del	XP_006721187.1:n.658+26_658+27del
NM_000078.3:c.658+26_658+27del MANE Select	NP_000069.2:n.658+26_658+27del
NM_001286085.2:c.658+26_658+27del	NP_001273014.1:n.658+26_658+27del