Canonical Allele Identifier: CA2807154686

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968962_56968971del , CM000678.2:g.56968962_56968971del	GRCh38
NC_000016.9:g.57002874_57002883del , CM000678.1:g.57002874_57002883del	GRCh37
NC_000016.8:g.55560375_55560384del	NCBI36
NG_008952.1:g.12040_12049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.234-424_234-415del MANE Select	ENSP00000200676.3:n.234-424_234-415del
ENST00000200676.7:c.234-424_234-415del	ENSP00000200676.3:n.234-424_234-415del
ENST00000379780.6:c.234-424_234-415del	ENSP00000369106.2:n.234-424_234-415del
ENST00000566128.1:c.39-424_39-415del	ENSP00000456276.1:n.39-424_39-415del
ENST00000569082.1:n.232-424_232-415del
NM_000078.2:c.234-424_234-415del	NP_000069.2:n.234-424_234-415del
NM_001286085.1:c.234-424_234-415del	NP_001273014.1:n.234-424_234-415del
XM_006721124.2:c.234-424_234-415del	XP_006721187.1:n.234-424_234-415del
XM_006721124.3:c.234-424_234-415del	XP_006721187.1:n.234-424_234-415del
NM_000078.3:c.234-424_234-415del MANE Select	NP_000069.2:n.234-424_234-415del
NM_001286085.2:c.234-424_234-415del	NP_001273014.1:n.234-424_234-415del