Canonical Allele Identifier: CA977671156

Gene: CETP

Linked Data

• gnomAD v3: 16-56968755-C-CTTTTTTTT
• gnomAD v4: 16-56968755-C-CTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968756_56968757insTTTTTTTT , CM000678.2:g.56968756_56968757insTTTTTTTT	GRCh38
NC_000016.9:g.57002668_57002669insTTTTTTTT , CM000678.1:g.57002668_57002669insTTTTTTTT	GRCh37
NC_000016.8:g.55560169_55560170insTTTTTTTT	NCBI36
NG_008952.1:g.11834_11835insTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-630_234-629insTTTTTTTT MANE Select	ENSP00000200676.3:n.234-630_234-629insTTTTTTTT
ENST00000200676.7:c.234-630_234-629insTTTTTTTT	ENSP00000200676.3:n.234-630_234-629insTTTTTTTT
ENST00000379780.6:c.234-630_234-629insTTTTTTTT	ENSP00000369106.2:n.234-630_234-629insTTTTTTTT
ENST00000566128.1:c.39-630_39-629insTTTTTTTT	ENSP00000456276.1:n.39-630_39-629insTTTTTTTT
ENST00000569082.1:n.232-630_232-629insTTTTTTTT
NM_000078.2:c.234-630_234-629insTTTTTTTT	NP_000069.2:n.234-630_234-629insTTTTTTTT
NM_001286085.1:c.234-630_234-629insTTTTTTTT	NP_001273014.1:n.234-630_234-629insTTTTTTTT
XM_006721124.2:c.234-630_234-629insTTTTTTTT	XP_006721187.1:n.234-630_234-629insTTTTTTTT
XM_006721124.3:c.234-630_234-629insTTTTTTTT	XP_006721187.1:n.234-630_234-629insTTTTTTTT
NM_000078.3:c.234-630_234-629insTTTTTTTT MANE Select	NP_000069.2:n.234-630_234-629insTTTTTTTT
NM_001286085.2:c.234-630_234-629insTTTTTTTT	NP_001273014.1:n.234-630_234-629insTTTTTTTT