Canonical Allele Identifier: CA8070942

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56969934C>T , CM000678.2:g.56969934C>T	GRCh38
NC_000016.9:g.57003846C>T , CM000678.1:g.57003846C>T	GRCh37
NC_000016.8:g.55561347C>T	NCBI36
NG_008952.1:g.13012C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000078.3:c.460C>T MANE Select	NP_000069.2:p.Arg154Trp
ENST00000200676.8:c.460C>T MANE Select	ENSP00000200676.3:p.Arg154Trp
NM_000078.2:c.460C>T	NP_000069.2:p.Arg154Trp
NM_001286085.1:c.460C>T	NP_001273014.1:p.Arg154Trp
NM_001286085.2:c.460C>T	NP_001273014.1:p.Arg154Trp
ENST00000200676.7:c.460C>T	ENSP00000200676.3:p.Arg154Trp
ENST00000379780.6:c.460C>T	ENSP00000369106.2:p.Arg154Trp
ENST00000566128.1:c.265C>T	ENSP00000456276.1:p.Arg89Trp
ENST00000569082.1:n.458C>T
XM_006721124.2:c.460C>T	XP_006721187.1:p.Arg154Trp
XM_006721124.3:c.460C>T	XP_006721187.1:p.Arg154Trp