Canonical Allele Identifier: CA2224395617
Gene: CETP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968744_56968745delinsTG , CM000678.2:g.56968744_56968745delinsTG GRCh38
NC_000016.9:g.57002656_57002657delinsTG , CM000678.1:g.57002656_57002657delinsTG GRCh37
NC_000016.8:g.55560157_55560158delinsTG NCBI36
NG_008952.1:g.11822_11823delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-642_234-641delinsTG MANE Select ENSP00000200676.3:n.234-642_234-641delins...
ENST00000200676.7:c.234-642_234-641delinsTG ENSP00000200676.3:n.234-642_234-641delins...
ENST00000379780.6:c.234-642_234-641delinsTG ENSP00000369106.2:n.234-642_234-641delins...
ENST00000566128.1:c.39-642_39-641delinsTG ENSP00000456276.1:n.39-642_39-641delinsTG...
ENST00000569082.1:n.232-642_232-641delinsTG
NM_000078.2:c.234-642_234-641delinsTG NP_000069.2:n.234-642_234-641delinsTG
NM_001286085.1:c.234-642_234-641delinsTG NP_001273014.1:n.234-642_234-641delinsTG
XM_006721124.2:c.234-642_234-641delinsTG XP_006721187.1:n.234-642_234-641delinsTG
XM_006721124.3:c.234-642_234-641delinsTG XP_006721187.1:n.234-642_234-641delinsTG
NM_000078.3:c.234-642_234-641delinsTG MANE Select NP_000069.2:n.234-642_234-641delinsTG
NM_001286085.2:c.234-642_234-641delinsTG NP_001273014.1:n.234-642_234-641delinsTG
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