Canonical Allele Identifier: CA2224395681
Gene: CETP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968861_56968865delinsACTTC , CM000678.2:g.56968861_56968865delinsACTTC GRCh38
NC_000016.9:g.57002773_57002777delinsACTTC , CM000678.1:g.57002773_57002777delinsACTTC GRCh37
NC_000016.8:g.55560274_55560278delinsACTTC NCBI36
NG_008952.1:g.11939_11943delinsACTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-525_234-521delinsACTTC MANE Select ENSP00000200676.3:n.234-525_234-521delins...
ENST00000200676.7:c.234-525_234-521delinsACTTC ENSP00000200676.3:n.234-525_234-521delins...
ENST00000379780.6:c.234-525_234-521delinsACTTC ENSP00000369106.2:n.234-525_234-521delins...
ENST00000566128.1:c.39-525_39-521delinsACTTC ENSP00000456276.1:n.39-525_39-521delinsAC...
ENST00000569082.1:n.232-525_232-521delinsACTTC
NM_000078.2:c.234-525_234-521delinsACTTC NP_000069.2:n.234-525_234-521delinsACTTC
NM_001286085.1:c.234-525_234-521delinsACTTC NP_001273014.1:n.234-525_234-521delinsACT...
XM_006721124.2:c.234-525_234-521delinsACTTC XP_006721187.1:n.234-525_234-521delinsACT...
XM_006721124.3:c.234-525_234-521delinsACTTC XP_006721187.1:n.234-525_234-521delinsACT...
NM_000078.3:c.234-525_234-521delinsACTTC MANE Select NP_000069.2:n.234-525_234-521delinsACTTC
NM_001286085.2:c.234-525_234-521delinsACTTC NP_001273014.1:n.234-525_234-521delinsACT...