Canonical Allele Identifier: CA2633386132
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56971474-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56971474C>A , CM000678.2:g.56971474C>A GRCh38
NC_000016.9:g.57005386C>A , CM000678.1:g.57005386C>A GRCh37
NC_000016.8:g.55562887C>A NCBI36
NG_008952.1:g.14552C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.658+93C>A MANE Select ENSP00000200676.3:n.658+93C>A
ENST00000200676.7:c.658+93C>A ENSP00000200676.3:n.658+93C>A
ENST00000379780.6:c.658+93C>A ENSP00000369106.2:n.658+93C>A
ENST00000566128.1:c.463+93C>A ENSP00000456276.1:n.463+93C>A
ENST00000569082.1:n.760+93C>A
NM_000078.2:c.658+93C>A NP_000069.2:n.658+93C>A
NM_001286085.1:c.658+93C>A NP_001273014.1:n.658+93C>A
XM_006721124.2:c.658+93C>A XP_006721187.1:n.658+93C>A
XM_006721124.3:c.658+93C>A XP_006721187.1:n.658+93C>A
NM_000078.3:c.658+93C>A MANE Select NP_000069.2:n.658+93C>A
NM_001286085.2:c.658+93C>A NP_001273014.1:n.658+93C>A
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