Canonical Allele Identifier: CA396008353
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56983409-G-A
MyVariant Identifiers: chr16:g.57017321G>A (hg19) chr16:g.56983409G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983409G>A , CM000678.2:g.56983409G>A GRCh38
NC_000016.9:g.57017321G>A , CM000678.1:g.57017321G>A GRCh37
NC_000016.8:g.55574822G>A NCBI36
NG_008952.1:g.26487G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1405G>A MANE Select ENSP00000200676.3:p.Asp469Asn
ENST00000200676.7:c.1405G>A ENSP00000200676.3:p.Asp469Asn
ENST00000379780.6:c.1225G>A ENSP00000369106.2:p.Asp409Asn
ENST00000566128.1:c.1210G>A ENSP00000456276.1:p.Asp404Asn
NM_000078.2:c.1405G>A NP_000069.2:p.Asp469Asn
NM_001286085.1:c.1225G>A NP_001273014.1:p.Asp409Asn
NM_000078.3:c.1405G>A MANE Select NP_000069.2:p.Asp469Asn
NM_001286085.2:c.1225G>A NP_001273014.1:p.Asp409Asn
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