Canonical Allele Identifier: CA396008011
Gene: CETP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.57017241T>A (hg19) chr16:g.56983329T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983329T>A , CM000678.2:g.56983329T>A GRCh38
NC_000016.9:g.57017241T>A , CM000678.1:g.57017241T>A GRCh37
NC_000016.8:g.55574742T>A NCBI36
NG_008952.1:g.26407T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1325T>A MANE Select ENSP00000200676.3:p.Leu442His
ENST00000650358.1:n.1723T>A
ENST00000200676.7:c.1325T>A ENSP00000200676.3:p.Leu442His
ENST00000379780.6:c.1145T>A ENSP00000369106.2:p.Leu382His
ENST00000566128.1:c.1130T>A ENSP00000456276.1:p.Leu377His
NM_000078.2:c.1325T>A NP_000069.2:p.Leu442His
NM_001286085.1:c.1145T>A NP_001273014.1:p.Leu382His
NM_000078.3:c.1325T>A MANE Select NP_000069.2:p.Leu442His
NM_001286085.2:c.1145T>A NP_001273014.1:p.Leu382His
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