Canonical Allele Identifier: CA2224402601
Gene: CETP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983477G= , CM000678.2:g.56983477G= GRCh38
NC_000016.9:g.57017389G= , CM000678.1:g.57017389G= GRCh37
NC_000016.8:g.55574890G= NCBI36
NG_008952.1:g.26555G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1407+66G= MANE Select ENSP00000200676.3:n.1407+66G=
ENST00000200676.7:c.1407+66G= ENSP00000200676.3:n.1407+66G=
ENST00000379780.6:c.1227+66G= ENSP00000369106.2:n.1227+66G=
ENST00000566128.1:c.1212+66G= ENSP00000456276.1:n.1212+66G=
NM_000078.2:c.1407+66G= NP_000069.2:n.1407+66G=
NM_001286085.1:c.1227+66G= NP_001273014.1:n.1227+66G=
NM_000078.3:c.1407+66G= MANE Select NP_000069.2:n.1407+66G=
NM_001286085.2:c.1227+66G= NP_001273014.1:n.1227+66G=
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