Canonical Allele Identifier: CA2224402577
Gene: CETP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983431C= , CM000678.2:g.56983431C= GRCh38
NC_000016.9:g.57017343C= , CM000678.1:g.57017343C= GRCh37
NC_000016.8:g.55574844C= NCBI36
NG_008952.1:g.26509C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1407+20C= MANE Select ENSP00000200676.3:n.1407+20C=
ENST00000200676.7:c.1407+20C= ENSP00000200676.3:n.1407+20C=
ENST00000379780.6:c.1227+20C= ENSP00000369106.2:n.1227+20C=
ENST00000566128.1:c.1212+20C= ENSP00000456276.1:n.1212+20C=
NM_000078.2:c.1407+20C= NP_000069.2:n.1407+20C=
NM_001286085.1:c.1227+20C= NP_001273014.1:n.1227+20C=
NM_000078.3:c.1407+20C= MANE Select NP_000069.2:n.1407+20C=
NM_001286085.2:c.1227+20C= NP_001273014.1:n.1227+20C=
Search 100 bp 5'
Search 100 bp 3'