Canonical Allele Identifier: CA2224401972
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056192296
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982085_56982094del , CM000678.2:g.56982085_56982094del GRCh38
NC_000016.9:g.57015997_57016006del , CM000678.1:g.57015997_57016006del GRCh37
NC_000016.8:g.55573498_55573507del NCBI36
NG_008952.1:g.25163_25172del

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-80_1249-71del MANE Select ENSP00000200676.3:n.1249-80_1249-71del
ENST00000650358.1:n.1647-80_1647-71del
ENST00000200676.7:c.1249-80_1249-71del ENSP00000200676.3:n.1249-80_1249-71del
ENST00000379780.6:c.1069-80_1069-71del ENSP00000369106.2:n.1069-80_1069-71del
ENST00000566128.1:c.1054-80_1054-71del ENSP00000456276.1:n.1054-80_1054-71del
NM_000078.2:c.1249-80_1249-71del NP_000069.2:n.1249-80_1249-71del
NM_001286085.1:c.1069-80_1069-71del NP_001273014.1:n.1069-80_1069-71del
NM_000078.3:c.1249-80_1249-71del MANE Select NP_000069.2:n.1249-80_1249-71del
NM_001286085.2:c.1069-80_1069-71del NP_001273014.1:n.1069-80_1069-71del
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