Canonical Allele Identifier: CA2580605728

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56962376G>T , CM000678.2:g.56962376G>T	GRCh38
NC_000016.9:g.56996288G>T , CM000678.1:g.56996288G>T	GRCh37
NC_000016.8:g.55553789G>T	NCBI36
NG_008952.1:g.5454G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000078.3:c.118+279G>T MANE Select	NP_000069.2:n.118+279G>T
ENST00000200676.8:c.118+279G>T MANE Select	ENSP00000200676.3:n.118+279G>T
NM_000078.2:c.118+279G>T	NP_000069.2:n.118+279G>T
NM_001286085.1:c.118+279G>T	NP_001273014.1:n.118+279G>T
NM_001286085.2:c.118+279G>T	NP_001273014.1:n.118+279G>T
ENST00000200676.7:c.118+279G>T	ENSP00000200676.3:n.118+279G>T
ENST00000379780.6:c.118+279G>T	ENSP00000369106.2:n.118+279G>T
ENST00000566128.1:c.-78+80G>T	ENSP00000456276.1:n.-78+80G>T
ENST00000569082.1:n.116+279G>T
XM_006721124.2:c.118+279G>T	XP_006721187.1:n.118+279G>T
XM_006721124.3:c.118+279G>T	XP_006721187.1:n.118+279G>T