Canonical Allele Identifier: CA396008001

Gene: CETP

Linked Data

• MyVariant Identifiers: chr16:g.57017238G>C (hg19) ; chr16:g.56983326G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983326G>C , CM000678.2:g.56983326G>C	GRCh38
NC_000016.9:g.57017238G>C , CM000678.1:g.57017238G>C	GRCh37
NC_000016.8:g.55574739G>C	NCBI36
NG_008952.1:g.26404G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1322G>C MANE Select	ENSP00000200676.3:p.Arg441Pro
ENST00000650358.1:n.1720G>C
ENST00000200676.7:c.1322G>C	ENSP00000200676.3:p.Arg441Pro
ENST00000379780.6:c.1142G>C	ENSP00000369106.2:p.Arg381Pro
ENST00000566128.1:c.1127G>C	ENSP00000456276.1:p.Arg376Pro
NM_000078.2:c.1322G>C	NP_000069.2:p.Arg441Pro
NM_001286085.1:c.1142G>C	NP_001273014.1:p.Arg381Pro
NM_000078.3:c.1322G>C MANE Select	NP_000069.2:p.Arg441Pro
NM_001286085.2:c.1142G>C	NP_001273014.1:p.Arg381Pro