Canonical Allele Identifier: CA396008058
Gene: CETP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.57017253T>A (hg19) chr16:g.56983341T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983341T>A , CM000678.2:g.56983341T>A GRCh38
NC_000016.9:g.57017253T>A , CM000678.1:g.57017253T>A GRCh37
NC_000016.8:g.55574754T>A NCBI36
NG_008952.1:g.26419T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1337T>A MANE Select ENSP00000200676.3:p.Phe446Tyr
ENST00000650358.1:n.1735T>A
ENST00000200676.7:c.1337T>A ENSP00000200676.3:p.Phe446Tyr
ENST00000379780.6:c.1157T>A ENSP00000369106.2:p.Phe386Tyr
ENST00000566128.1:c.1142T>A ENSP00000456276.1:p.Phe381Tyr
NM_000078.2:c.1337T>A NP_000069.2:p.Phe446Tyr
NM_001286085.1:c.1157T>A NP_001273014.1:p.Phe386Tyr
NM_000078.3:c.1337T>A MANE Select NP_000069.2:p.Phe446Tyr
NM_001286085.2:c.1157T>A NP_001273014.1:p.Phe386Tyr
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