Canonical Allele Identifier: CA2224401994

Gene: CETP

Linked Data

• dbSNP Id: rs2056192678

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56982136A>T , CM000678.2:g.56982136A>T	GRCh38
NC_000016.9:g.57016048A>T , CM000678.1:g.57016048A>T	GRCh37
NC_000016.8:g.55573549A>T	NCBI36
NG_008952.1:g.25214A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1249-29A>T MANE Select	ENSP00000200676.3:n.1249-29A>T
ENST00000650358.1:n.1647-29A>T
ENST00000200676.7:c.1249-29A>T	ENSP00000200676.3:n.1249-29A>T
ENST00000379780.6:c.1069-29A>T	ENSP00000369106.2:n.1069-29A>T
ENST00000566128.1:c.1054-29A>T	ENSP00000456276.1:n.1054-29A>T
NM_000078.2:c.1249-29A>T	NP_000069.2:n.1249-29A>T
NM_001286085.1:c.1069-29A>T	NP_001273014.1:n.1069-29A>T
NM_000078.3:c.1249-29A>T MANE Select	NP_000069.2:n.1249-29A>T
NM_001286085.2:c.1069-29A>T	NP_001273014.1:n.1069-29A>T