Canonical Allele Identifier: CA495622694

Gene: CETP

Linked Data

• gnomAD v4: 16-56983408-A-T
• MyVariant Identifiers: chr16:g.57017320A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983408A>T , CM000678.2:g.56983408A>T	GRCh38
NC_000016.9:g.57017320A>T , CM000678.1:g.57017320A>T	GRCh37
NC_000016.8:g.55574821A>T	NCBI36
NG_008952.1:g.26486A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1404A>T MANE Select	ENSP00000200676.3:p.Arg468=
ENST00000200676.7:c.1404A>T	ENSP00000200676.3:p.Arg468=
ENST00000379780.6:c.1224A>T	ENSP00000369106.2:p.Arg408=
ENST00000566128.1:c.1209A>T	ENSP00000456276.1:p.Arg403=
NM_000078.2:c.1404A>T	NP_000069.2:p.Arg468=
NM_001286085.1:c.1224A>T	NP_001273014.1:p.Arg408=
NM_000078.3:c.1404A>T MANE Select	NP_000069.2:p.Arg468=
NM_001286085.2:c.1224A>T	NP_001273014.1:p.Arg408=