Canonical Allele Identifier: CA2224401981
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982101G= , CM000678.2:g.56982101G= GRCh38
NC_000016.9:g.57016013G= , CM000678.1:g.57016013G= GRCh37
NC_000016.8:g.55573514G= NCBI36
NG_008952.1:g.25179G=

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-64G= MANE Select ENSP00000200676.3:n.1249-64G=
ENST00000650358.1:n.1647-64G=
ENST00000200676.7:c.1249-64G= ENSP00000200676.3:n.1249-64G=
ENST00000379780.6:c.1069-64G= ENSP00000369106.2:n.1069-64G=
ENST00000566128.1:c.1054-64G= ENSP00000456276.1:n.1054-64G=
NM_000078.2:c.1249-64G= NP_000069.2:n.1249-64G=
NM_001286085.1:c.1069-64G= NP_001273014.1:n.1069-64G=
NM_000078.3:c.1249-64G= MANE Select NP_000069.2:n.1249-64G=
NM_001286085.2:c.1069-64G= NP_001273014.1:n.1069-64G=