Canonical Allele Identifier: CA2633388534

Gene: CETP

Linked Data

• gnomAD v4: 16-56983458-G-GCCCAGACAGGATTCCTGGGGTGACTGGGGGCTGTTGGGGAGACAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983460_56983505dup , CM000678.2:g.56983460_56983505dup	GRCh38
NC_000016.9:g.57017372_57017417dup , CM000678.1:g.57017372_57017417dup	GRCh37
NC_000016.8:g.55574873_55574918dup	NCBI36
NG_008952.1:g.26538_26583dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1407+49_1408-87dup MANE Select	ENSP00000200676.3:n.1407+49_1408-87dup
ENST00000200676.7:c.1407+49_1408-87dup	ENSP00000200676.3:n.1407+49_1408-87dup
ENST00000379780.6:c.1227+49_1228-87dup	ENSP00000369106.2:n.1227+49_1228-87dup
ENST00000566128.1:c.1212+49_1213-87dup	ENSP00000456276.1:n.1212+49_1213-87dup
NM_000078.2:c.1407+49_1408-87dup	NP_000069.2:n.1407+49_1408-87dup
NM_001286085.1:c.1227+49_1228-87dup	NP_001273014.1:n.1227+49_1228-87dup
NM_000078.3:c.1407+49_1408-87dup MANE Select	NP_000069.2:n.1407+49_1408-87dup
NM_001286085.2:c.1227+49_1228-87dup	NP_001273014.1:n.1227+49_1228-87dup