Canonical Allele Identifier: CA2576002901
Gene: CETP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56975027T>C , CM000678.2:g.56975027T>C GRCh38
NC_000016.9:g.57008939T>C , CM000678.1:g.57008939T>C GRCh37
NC_000016.8:g.55566440T>C NCBI36
NG_008952.1:g.18105T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.931-74T>C MANE Select ENSP00000200676.3:n.931-74T>C
ENST00000200676.7:c.931-74T>C ENSP00000200676.3:n.931-74T>C
ENST00000379780.6:c.751-74T>C ENSP00000369106.2:n.751-74T>C
ENST00000566128.1:c.736-74T>C ENSP00000456276.1:n.736-74T>C
NM_000078.2:c.931-74T>C NP_000069.2:n.931-74T>C
NM_001286085.1:c.751-74T>C NP_001273014.1:n.751-74T>C
NM_000078.3:c.931-74T>C MANE Select NP_000069.2:n.931-74T>C
NM_001286085.2:c.751-74T>C NP_001273014.1:n.751-74T>C
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