Canonical Allele Identifier: CA2633388479

Gene: CETP

Linked Data

• gnomAD v4: 16-56983423-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983429del , CM000678.2:g.56983429del	GRCh38
NC_000016.9:g.57017341del , CM000678.1:g.57017341del	GRCh37
NC_000016.8:g.55574842del	NCBI36
NG_008952.1:g.26507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1407+18del MANE Select	ENSP00000200676.3:n.1407+18del
ENST00000200676.7:c.1407+18del	ENSP00000200676.3:n.1407+18del
ENST00000379780.6:c.1227+18del	ENSP00000369106.2:n.1227+18del
ENST00000566128.1:c.1212+18del	ENSP00000456276.1:n.1212+18del
NM_000078.2:c.1407+18del	NP_000069.2:n.1407+18del
NM_001286085.1:c.1227+18del	NP_001273014.1:n.1227+18del
NM_000078.3:c.1407+18del MANE Select	NP_000069.2:n.1407+18del
NM_001286085.2:c.1227+18del	NP_001273014.1:n.1227+18del