Canonical Allele Identifier: CA977671017

Gene: CETP

Linked Data

• gnomAD v3: 16-56968729-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTT
• gnomAD v4: 16-56968729-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968744_56968745insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000678.2:g.56968744_56968745insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000016.9:g.57002656_57002657insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000678.1:g.57002656_57002657insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000016.8:g.55560157_55560158insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_008952.1:g.11822_11823insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000200676.3:n.234-642_234-641insTTT...
ENST00000200676.7:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000200676.3:n.234-642_234-641insTTT...
ENST00000379780.6:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000369106.2:n.234-642_234-641insTTT...
ENST00000566128.1:c.39-642_39-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000456276.1:n.39-642_39-641insTTTTT...
ENST00000569082.1:n.232-642_232-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000078.2:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000069.2:n.234-642_234-641insTTTTTTTTT...
NM_001286085.1:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001273014.1:n.234-642_234-641insTTTTTT...
XM_006721124.2:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006721187.1:n.234-642_234-641insTTTTTT...
XM_006721124.3:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006721187.1:n.234-642_234-641insTTTTTT...
NM_000078.3:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000069.2:n.234-642_234-641insTTTTTTTTT...
NM_001286085.2:c.234-642_234-641insTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001273014.1:n.234-642_234-641insTTTTTT...