Canonical Allele Identifier: CA2224401971
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982082_56982092delinsTGCTTGTCCAG , CM000678.2:g.56982082_56982092delinsTGCTTGTCCAG GRCh38
NC_000016.9:g.57015994_57016004delinsTGCTTGTCCAG , CM000678.1:g.57015994_57016004delinsTGCTTGTCCAG GRCh37
NC_000016.8:g.55573495_55573505delinsTGCTTGTCCAG NCBI36
NG_008952.1:g.25160_25170delinsTGCTTGTCCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-83_1249-73delinsTGCTTGTCCAG MANE Select ENSP00000200676.3:n.1249-83_1249-73delins...
ENST00000650358.1:n.1647-83_1647-73delinsTGCTTGTCCAG
ENST00000200676.7:c.1249-83_1249-73delinsTGCTTGTCCAG ENSP00000200676.3:n.1249-83_1249-73delins...
ENST00000379780.6:c.1069-83_1069-73delinsTGCTTGTCCAG ENSP00000369106.2:n.1069-83_1069-73delins...
ENST00000566128.1:c.1054-83_1054-73delinsTGCTTGTCCAG ENSP00000456276.1:n.1054-83_1054-73delins...
NM_000078.2:c.1249-83_1249-73delinsTGCTTGTCCAG NP_000069.2:n.1249-83_1249-73delinsTGCTTG...
NM_001286085.1:c.1069-83_1069-73delinsTGCTTGTCCAG NP_001273014.1:n.1069-83_1069-73delinsTGC...
NM_000078.3:c.1249-83_1249-73delinsTGCTTGTCCAG MANE Select NP_000069.2:n.1249-83_1249-73delinsTGCTTG...
NM_001286085.2:c.1069-83_1069-73delinsTGCTTGTCCAG NP_001273014.1:n.1069-83_1069-73delinsTGC...