Canonical Allele Identifier: CA2224401945

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56982022_56982023delinsTG , CM000678.2:g.56982022_56982023delinsTG	GRCh38
NC_000016.9:g.57015934_57015935delinsTG , CM000678.1:g.57015934_57015935delinsTG	GRCh37
NC_000016.8:g.55573435_55573436delinsTG	NCBI36
NG_008952.1:g.25100_25101delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1249-143_1249-142delinsTG MANE Select	ENSP00000200676.3:n.1249-143_1249-142delinsTG
ENST00000650358.1:n.1647-143_1647-142delinsTG
ENST00000200676.7:c.1249-143_1249-142delinsTG	ENSP00000200676.3:n.1249-143_1249-142delinsTG
ENST00000379780.6:c.1069-143_1069-142delinsTG	ENSP00000369106.2:n.1069-143_1069-142delinsTG
ENST00000566128.1:c.1054-143_1054-142delinsTG	ENSP00000456276.1:n.1054-143_1054-142delinsTG
NM_000078.2:c.1249-143_1249-142delinsTG	NP_000069.2:n.1249-143_1249-142delinsTG
NM_001286085.1:c.1069-143_1069-142delinsTG	NP_001273014.1:n.1069-143_1069-142delinsTG
NM_000078.3:c.1249-143_1249-142delinsTG MANE Select	NP_000069.2:n.1249-143_1249-142delinsTG
NM_001286085.2:c.1069-143_1069-142delinsTG	NP_001273014.1:n.1069-143_1069-142delinsTG