Canonical Allele Identifier: CA2633387207
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56982076-GATGA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982080_56982083del , CM000678.2:g.56982080_56982083del GRCh38
NC_000016.9:g.57015992_57015995del , CM000678.1:g.57015992_57015995del GRCh37
NC_000016.8:g.55573493_55573496del NCBI36
NG_008952.1:g.25158_25161del

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-85_1249-82del MANE Select ENSP00000200676.3:n.1249-85_1249-82del
ENST00000650358.1:n.1647-85_1647-82del
ENST00000200676.7:c.1249-85_1249-82del ENSP00000200676.3:n.1249-85_1249-82del
ENST00000379780.6:c.1069-85_1069-82del ENSP00000369106.2:n.1069-85_1069-82del
ENST00000566128.1:c.1054-85_1054-82del ENSP00000456276.1:n.1054-85_1054-82del
NM_000078.2:c.1249-85_1249-82del NP_000069.2:n.1249-85_1249-82del
NM_001286085.1:c.1069-85_1069-82del NP_001273014.1:n.1069-85_1069-82del
NM_000078.3:c.1249-85_1249-82del MANE Select NP_000069.2:n.1249-85_1249-82del
NM_001286085.2:c.1069-85_1069-82del NP_001273014.1:n.1069-85_1069-82del
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