Canonical Allele Identifier: CA2633386116
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56971467-CACTCTTCCTGTCTAGGTCCCA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56971468_56971488del , CM000678.2:g.56971468_56971488del GRCh38
NC_000016.9:g.57005380_57005400del , CM000678.1:g.57005380_57005400del GRCh37
NC_000016.8:g.55562881_55562901del NCBI36
NG_008952.1:g.14546_14566del

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.658+87_658+107del MANE Select ENSP00000200676.3:n.658+87_658+107del
ENST00000200676.7:c.658+87_658+107del ENSP00000200676.3:n.658+87_658+107del
ENST00000379780.6:c.658+87_658+107del ENSP00000369106.2:n.658+87_658+107del
ENST00000566128.1:c.463+87_463+107del ENSP00000456276.1:n.463+87_463+107del
ENST00000569082.1:n.760+87_760+107del
NM_000078.2:c.658+87_658+107del NP_000069.2:n.658+87_658+107del
NM_001286085.1:c.658+87_658+107del NP_001273014.1:n.658+87_658+107del
XM_006721124.2:c.658+87_658+107del XP_006721187.1:n.658+87_658+107del
XM_006721124.3:c.658+87_658+107del XP_006721187.1:n.658+87_658+107del
NM_000078.3:c.658+87_658+107del MANE Select NP_000069.2:n.658+87_658+107del
NM_001286085.2:c.658+87_658+107del NP_001273014.1:n.658+87_658+107del
Search 100 bp 5'
Search 100 bp 3'