Canonical Allele Identifier: CA281521323

Gene: CETP

Linked Data

• dbSNP Id: rs747845015
• MyVariant Identifiers: chr16:g.57002879_57002880insG (hg19) ; chr16:g.56968967_56968968insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968969dup , CM000678.2:g.56968969dup	GRCh38
NC_000016.9:g.57002881dup , CM000678.1:g.57002881dup	GRCh37
NC_000016.8:g.55560382dup	NCBI36
NG_008952.1:g.12047dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-417dup MANE Select	ENSP00000200676.3:n.234-417dup
ENST00000200676.7:c.234-417dup	ENSP00000200676.3:n.234-417dup
ENST00000379780.6:c.234-417dup	ENSP00000369106.2:n.234-417dup
ENST00000566128.1:c.39-417dup	ENSP00000456276.1:n.39-417dup
ENST00000569082.1:n.232-417dup
NM_000078.2:c.234-417dup	NP_000069.2:n.234-417dup
NM_001286085.1:c.234-417dup	NP_001273014.1:n.234-417dup
XM_006721124.2:c.234-417dup	XP_006721187.1:n.234-417dup
XM_006721124.3:c.234-417dup	XP_006721187.1:n.234-417dup
NM_000078.3:c.234-417dup MANE Select	NP_000069.2:n.234-417dup
NM_001286085.2:c.234-417dup	NP_001273014.1:n.234-417dup