Canonical Allele Identifier: CA2224401997
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982139A= , CM000678.2:g.56982139A= GRCh38
NC_000016.9:g.57016051A= , CM000678.1:g.57016051A= GRCh37
NC_000016.8:g.55573552A= NCBI36
NG_008952.1:g.25217A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1249-26A= MANE Select ENSP00000200676.3:n.1249-26A=
ENST00000650358.1:n.1647-26A=
ENST00000200676.7:c.1249-26A= ENSP00000200676.3:n.1249-26A=
ENST00000379780.6:c.1069-26A= ENSP00000369106.2:n.1069-26A=
ENST00000566128.1:c.1054-26A= ENSP00000456276.1:n.1054-26A=
NM_000078.2:c.1249-26A= NP_000069.2:n.1249-26A=
NM_001286085.1:c.1069-26A= NP_001273014.1:n.1069-26A=
NM_000078.3:c.1249-26A= MANE Select NP_000069.2:n.1249-26A=
NM_001286085.2:c.1069-26A= NP_001273014.1:n.1069-26A=