Canonical Allele Identifier: CA977671276
Gene: CETP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968831A>T , CM000678.2:g.56968831A>T GRCh38
NC_000016.9:g.57002743A>T , CM000678.1:g.57002743A>T GRCh37
NC_000016.8:g.55560244A>T NCBI36
NG_008952.1:g.11909A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-555A>T MANE Select ENSP00000200676.3:n.234-555A>T
ENST00000200676.7:c.234-555A>T ENSP00000200676.3:n.234-555A>T
ENST00000379780.6:c.234-555A>T ENSP00000369106.2:n.234-555A>T
ENST00000566128.1:c.39-555A>T ENSP00000456276.1:n.39-555A>T
ENST00000569082.1:n.232-555A>T
NM_000078.2:c.234-555A>T NP_000069.2:n.234-555A>T
NM_001286085.1:c.234-555A>T NP_001273014.1:n.234-555A>T
XM_006721124.2:c.234-555A>T XP_006721187.1:n.234-555A>T
XM_006721124.3:c.234-555A>T XP_006721187.1:n.234-555A>T
NM_000078.3:c.234-555A>T MANE Select NP_000069.2:n.234-555A>T
NM_001286085.2:c.234-555A>T NP_001273014.1:n.234-555A>T