Canonical Allele Identifier: CA2224395691

Gene: CETP

Linked Data

• dbSNP Id: rs2056087331

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968889del , CM000678.2:g.56968889del	GRCh38
NC_000016.9:g.57002801del , CM000678.1:g.57002801del	GRCh37
NC_000016.8:g.55560302del	NCBI36
NG_008952.1:g.11967del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-497del MANE Select	ENSP00000200676.3:n.234-497del
ENST00000200676.7:c.234-497del	ENSP00000200676.3:n.234-497del
ENST00000379780.6:c.234-497del	ENSP00000369106.2:n.234-497del
ENST00000566128.1:c.39-497del	ENSP00000456276.1:n.39-497del
ENST00000569082.1:n.232-497del
NM_000078.2:c.234-497del	NP_000069.2:n.234-497del
NM_001286085.1:c.234-497del	NP_001273014.1:n.234-497del
XM_006721124.2:c.234-497del	XP_006721187.1:n.234-497del
XM_006721124.3:c.234-497del	XP_006721187.1:n.234-497del
NM_000078.3:c.234-497del MANE Select	NP_000069.2:n.234-497del
NM_001286085.2:c.234-497del	NP_001273014.1:n.234-497del