Canonical Allele Identifier: CA2224395674
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968840A= , CM000678.2:g.56968840A= GRCh38
NC_000016.9:g.57002752A= , CM000678.1:g.57002752A= GRCh37
NC_000016.8:g.55560253A= NCBI36
NG_008952.1:g.11918A=

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-546A= MANE Select ENSP00000200676.3:n.234-546A=
ENST00000200676.7:c.234-546A= ENSP00000200676.3:n.234-546A=
ENST00000379780.6:c.234-546A= ENSP00000369106.2:n.234-546A=
ENST00000566128.1:c.39-546A= ENSP00000456276.1:n.39-546A=
ENST00000569082.1:n.232-546A=
NM_000078.2:c.234-546A= NP_000069.2:n.234-546A=
NM_001286085.1:c.234-546A= NP_001273014.1:n.234-546A=
XM_006721124.2:c.234-546A= XP_006721187.1:n.234-546A=
XM_006721124.3:c.234-546A= XP_006721187.1:n.234-546A=
NM_000078.3:c.234-546A= MANE Select NP_000069.2:n.234-546A=
NM_001286085.2:c.234-546A= NP_001273014.1:n.234-546A=