Canonical Allele Identifier: CA2633387219
Gene: CETP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982082T>G , CM000678.2:g.56982082T>G GRCh38
NC_000016.9:g.57015994T>G , CM000678.1:g.57015994T>G GRCh37
NC_000016.8:g.55573495T>G NCBI36
NG_008952.1:g.25160T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-83T>G MANE Select ENSP00000200676.3:n.1249-83T>G
ENST00000650358.1:n.1647-83T>G
ENST00000200676.7:c.1249-83T>G ENSP00000200676.3:n.1249-83T>G
ENST00000379780.6:c.1069-83T>G ENSP00000369106.2:n.1069-83T>G
ENST00000566128.1:c.1054-83T>G ENSP00000456276.1:n.1054-83T>G
NM_000078.2:c.1249-83T>G NP_000069.2:n.1249-83T>G
NM_001286085.1:c.1069-83T>G NP_001273014.1:n.1069-83T>G
NM_000078.3:c.1249-83T>G MANE Select NP_000069.2:n.1249-83T>G
NM_001286085.2:c.1069-83T>G NP_001273014.1:n.1069-83T>G