Canonical Allele Identifier: CA396007983

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017236A>C (hg19) ; chr16:g.56983324A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983324A>C , CM000678.2:g.56983324A>C	GRCh38
NC_000016.9:g.57017236A>C , CM000678.1:g.57017236A>C	GRCh37
NC_000016.8:g.55574737A>C	NCBI36
NG_008952.1:g.26402A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1322-2A>C MANE Select	ENSP00000200676.3:n.1322-2A>C
ENST00000650358.1:n.1720-2A>C
ENST00000200676.7:c.1322-2A>C	ENSP00000200676.3:n.1322-2A>C
ENST00000379780.6:c.1142-2A>C	ENSP00000369106.2:n.1142-2A>C
ENST00000566128.1:c.1127-2A>C	ENSP00000456276.1:n.1127-2A>C
NM_000078.2:c.1322-2A>C	NP_000069.2:n.1322-2A>C
NM_001286085.1:c.1142-2A>C	NP_001273014.1:n.1142-2A>C
NM_000078.3:c.1322-2A>C MANE Select	NP_000069.2:n.1322-2A>C
NM_001286085.2:c.1142-2A>C	NP_001273014.1:n.1142-2A>C