Canonical Allele Identifier: CA2224402507
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983282T= , CM000678.2:g.56983282T= GRCh38
NC_000016.9:g.57017194T= , CM000678.1:g.57017194T= GRCh37
NC_000016.8:g.55574695T= NCBI36
NG_008952.1:g.26360T=

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1322-44T= MANE Select ENSP00000200676.3:n.1322-44T=
ENST00000650358.1:n.1720-44T=
ENST00000200676.7:c.1322-44T= ENSP00000200676.3:n.1322-44T=
ENST00000379780.6:c.1142-44T= ENSP00000369106.2:n.1142-44T=
ENST00000566128.1:c.1127-44T= ENSP00000456276.1:n.1127-44T=
NM_000078.2:c.1322-44T= NP_000069.2:n.1322-44T=
NM_001286085.1:c.1142-44T= NP_001273014.1:n.1142-44T=
NM_000078.3:c.1322-44T= MANE Select NP_000069.2:n.1322-44T=
NM_001286085.2:c.1142-44T= NP_001273014.1:n.1142-44T=