Canonical Allele Identifier: CA396008014
Gene: CETP HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1325T>C MANE Select ENSP00000200676.3:p.Leu442Pro
ENST00000650358.1:n.1723T>C
ENST00000200676.7:c.1325T>C ENSP00000200676.3:p.Leu442Pro
ENST00000379780.6:c.1145T>C ENSP00000369106.2:p.Leu382Pro
ENST00000566128.1:c.1130T>C ENSP00000456276.1:p.Leu377Pro
NM_000078.2:c.1325T>C NP_000069.2:p.Leu442Pro
NM_001286085.1:c.1145T>C NP_001273014.1:p.Leu382Pro
NM_000078.3:c.1325T>C MANE Select NP_000069.2:p.Leu442Pro
NM_001286085.2:c.1145T>C NP_001273014.1:p.Leu382Pro
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