Canonical Allele Identifier: CA2224395659

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968807_56968808delinsAC , CM000678.2:g.56968807_56968808delinsAC	GRCh38
NC_000016.9:g.57002719_57002720delinsAC , CM000678.1:g.57002719_57002720delinsAC	GRCh37
NC_000016.8:g.55560220_55560221delinsAC	NCBI36
NG_008952.1:g.11885_11886delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-579_234-578delinsAC MANE Select	ENSP00000200676.3:n.234-579_234-578delins...
ENST00000200676.7:c.234-579_234-578delinsAC	ENSP00000200676.3:n.234-579_234-578delins...
ENST00000379780.6:c.234-579_234-578delinsAC	ENSP00000369106.2:n.234-579_234-578delins...
ENST00000566128.1:c.39-579_39-578delinsAC	ENSP00000456276.1:n.39-579_39-578delinsAC...
ENST00000569082.1:n.232-579_232-578delinsAC
NM_000078.2:c.234-579_234-578delinsAC	NP_000069.2:n.234-579_234-578delinsAC
NM_001286085.1:c.234-579_234-578delinsAC	NP_001273014.1:n.234-579_234-578delinsAC
XM_006721124.2:c.234-579_234-578delinsAC	XP_006721187.1:n.234-579_234-578delinsAC
XM_006721124.3:c.234-579_234-578delinsAC	XP_006721187.1:n.234-579_234-578delinsAC
NM_000078.3:c.234-579_234-578delinsAC MANE Select	NP_000069.2:n.234-579_234-578delinsAC
NM_001286085.2:c.234-579_234-578delinsAC	NP_001273014.1:n.234-579_234-578delinsAC