Canonical Allele Identifier: CA2224395673
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056087040

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968832_56968843del , CM000678.2:g.56968832_56968843del GRCh38
NC_000016.9:g.57002744_57002755del , CM000678.1:g.57002744_57002755del GRCh37
NC_000016.8:g.55560245_55560256del NCBI36
NG_008952.1:g.11910_11921del

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-554_234-543del MANE Select ENSP00000200676.3:n.234-554_234-543del
ENST00000200676.7:c.234-554_234-543del ENSP00000200676.3:n.234-554_234-543del
ENST00000379780.6:c.234-554_234-543del ENSP00000369106.2:n.234-554_234-543del
ENST00000566128.1:c.39-554_39-543del ENSP00000456276.1:n.39-554_39-543del
ENST00000569082.1:n.232-554_232-543del
NM_000078.2:c.234-554_234-543del NP_000069.2:n.234-554_234-543del
NM_001286085.1:c.234-554_234-543del NP_001273014.1:n.234-554_234-543del
XM_006721124.2:c.234-554_234-543del XP_006721187.1:n.234-554_234-543del
XM_006721124.3:c.234-554_234-543del XP_006721187.1:n.234-554_234-543del
NM_000078.3:c.234-554_234-543del MANE Select NP_000069.2:n.234-554_234-543del
NM_001286085.2:c.234-554_234-543del NP_001273014.1:n.234-554_234-543del