Canonical Allele Identifier: CA977670864
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056085459
gnomAD v3: 16-56968659-CT-C
gnomAD v4: 16-56968659-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968663del , CM000678.2:g.56968663del GRCh38
NC_000016.9:g.57002575del , CM000678.1:g.57002575del GRCh37
NC_000016.8:g.55560076del NCBI36
NG_008952.1:g.11741del

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-723del MANE Select ENSP00000200676.3:n.234-723del
ENST00000200676.7:c.234-723del ENSP00000200676.3:n.234-723del
ENST00000379780.6:c.234-723del ENSP00000369106.2:n.234-723del
ENST00000566128.1:c.39-723del ENSP00000456276.1:n.39-723del
ENST00000569082.1:n.232-723del
NM_000078.2:c.234-723del NP_000069.2:n.234-723del
NM_001286085.1:c.234-723del NP_001273014.1:n.234-723del
XM_006721124.2:c.234-723del XP_006721187.1:n.234-723del
XM_006721124.3:c.234-723del XP_006721187.1:n.234-723del
NM_000078.3:c.234-723del MANE Select NP_000069.2:n.234-723del
NM_001286085.2:c.234-723del NP_001273014.1:n.234-723del
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