Canonical Allele Identifier: CA977671148

Gene: CETP

Linked Data

• gnomAD v3: 16-56968754-G-GTTTTTTT
• gnomAD v4: 16-56968754-G-GTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968754_56968755insTTTTTTT , CM000678.2:g.56968754_56968755insTTTTTTT	GRCh38
NC_000016.9:g.57002666_57002667insTTTTTTT , CM000678.1:g.57002666_57002667insTTTTTTT	GRCh37
NC_000016.8:g.55560167_55560168insTTTTTTT	NCBI36
NG_008952.1:g.11832_11833insTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-632_234-631insTTTTTTT MANE Select	ENSP00000200676.3:n.234-632_234-631insTTTTTTT
ENST00000200676.7:c.234-632_234-631insTTTTTTT	ENSP00000200676.3:n.234-632_234-631insTTTTTTT
ENST00000379780.6:c.234-632_234-631insTTTTTTT	ENSP00000369106.2:n.234-632_234-631insTTTTTTT
ENST00000566128.1:c.39-632_39-631insTTTTTTT	ENSP00000456276.1:n.39-632_39-631insTTTTTTT
ENST00000569082.1:n.232-632_232-631insTTTTTTT
NM_000078.2:c.234-632_234-631insTTTTTTT	NP_000069.2:n.234-632_234-631insTTTTTTT
NM_001286085.1:c.234-632_234-631insTTTTTTT	NP_001273014.1:n.234-632_234-631insTTTTTTT
XM_006721124.2:c.234-632_234-631insTTTTTTT	XP_006721187.1:n.234-632_234-631insTTTTTTT
XM_006721124.3:c.234-632_234-631insTTTTTTT	XP_006721187.1:n.234-632_234-631insTTTTTTT
NM_000078.3:c.234-632_234-631insTTTTTTT MANE Select	NP_000069.2:n.234-632_234-631insTTTTTTT
NM_001286085.2:c.234-632_234-631insTTTTTTT	NP_001273014.1:n.234-632_234-631insTTTTTTT