Canonical Allele Identifier: CA396008358
Gene: CETP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983410A>T , CM000678.2:g.56983410A>T GRCh38
NC_000016.9:g.57017322A>T , CM000678.1:g.57017322A>T GRCh37
NC_000016.8:g.55574823A>T NCBI36
NG_008952.1:g.26488A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1406A>T MANE Select ENSP00000200676.3:p.Asp469Val
ENST00000200676.7:c.1406A>T ENSP00000200676.3:p.Asp469Val
ENST00000379780.6:c.1226A>T ENSP00000369106.2:p.Asp409Val
ENST00000566128.1:c.1211A>T ENSP00000456276.1:p.Asp404Val
NM_000078.2:c.1406A>T NP_000069.2:p.Asp469Val
NM_001286085.1:c.1226A>T NP_001273014.1:p.Asp409Val
NM_000078.3:c.1406A>T MANE Select NP_000069.2:p.Asp469Val
NM_001286085.2:c.1226A>T NP_001273014.1:p.Asp409Val