Canonical Allele Identifier: CA2224400051
Gene: CETP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56975025C= , CM000678.2:g.56975025C= GRCh38
NC_000016.9:g.57008937C= , CM000678.1:g.57008937C= GRCh37
NC_000016.8:g.55566438C= NCBI36
NG_008952.1:g.18103C=

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.931-76C= MANE Select ENSP00000200676.3:n.931-76C=
ENST00000200676.7:c.931-76C= ENSP00000200676.3:n.931-76C=
ENST00000379780.6:c.751-76C= ENSP00000369106.2:n.751-76C=
ENST00000566128.1:c.736-76C= ENSP00000456276.1:n.736-76C=
NM_000078.2:c.931-76C= NP_000069.2:n.931-76C=
NM_001286085.1:c.751-76C= NP_001273014.1:n.751-76C=
NM_000078.3:c.931-76C= MANE Select NP_000069.2:n.931-76C=
NM_001286085.2:c.751-76C= NP_001273014.1:n.751-76C=
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