Canonical Allele Identifier: CA2224395672
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968831_56968843delinsATTTCATTCATAG , CM000678.2:g.56968831_56968843delinsATTTCATTCATAG GRCh38
NC_000016.9:g.57002743_57002755delinsATTTCATTCATAG , CM000678.1:g.57002743_57002755delinsATTTCATTCATAG GRCh37
NC_000016.8:g.55560244_55560256delinsATTTCATTCATAG NCBI36
NG_008952.1:g.11909_11921delinsATTTCATTCATAG

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-555_234-543delinsATTTCATTCATAG MANE Select ENSP00000200676.3:n.234-555_234-543delins...
ENST00000200676.7:c.234-555_234-543delinsATTTCATTCATAG ENSP00000200676.3:n.234-555_234-543delins...
ENST00000379780.6:c.234-555_234-543delinsATTTCATTCATAG ENSP00000369106.2:n.234-555_234-543delins...
ENST00000566128.1:c.39-555_39-543delinsATTTCATTCATAG ENSP00000456276.1:n.39-555_39-543delinsAT...
ENST00000569082.1:n.232-555_232-543delinsATTTCATTCATAG
NM_000078.2:c.234-555_234-543delinsATTTCATTCATAG NP_000069.2:n.234-555_234-543delinsATTTCA...
NM_001286085.1:c.234-555_234-543delinsATTTCATTCATAG NP_001273014.1:n.234-555_234-543delinsATT...
XM_006721124.2:c.234-555_234-543delinsATTTCATTCATAG XP_006721187.1:n.234-555_234-543delinsATT...
XM_006721124.3:c.234-555_234-543delinsATTTCATTCATAG XP_006721187.1:n.234-555_234-543delinsATT...
NM_000078.3:c.234-555_234-543delinsATTTCATTCATAG MANE Select NP_000069.2:n.234-555_234-543delinsATTTCA...
NM_001286085.2:c.234-555_234-543delinsATTTCATTCATAG NP_001273014.1:n.234-555_234-543delinsATT...