Canonical Allele Identifier: CA722011022

Gene: CETP

Linked Data

• dbSNP Id: rs1299002240
• MyVariant Identifiers: chr16:g.57017409_57017418del (hg19) ; chr16:g.56983497_56983506del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983500_56983509del , CM000678.2:g.56983500_56983509del	GRCh38
NC_000016.9:g.57017412_57017421del , CM000678.1:g.57017412_57017421del	GRCh37
NC_000016.8:g.55574913_55574922del	NCBI36
NG_008952.1:g.26578_26587del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1407+89_1408-83del MANE Select	ENSP00000200676.3:n.1407+89_1408-83del
ENST00000200676.7:c.1407+89_1408-83del	ENSP00000200676.3:n.1407+89_1408-83del
ENST00000379780.6:c.1227+89_1228-83del	ENSP00000369106.2:n.1227+89_1228-83del
ENST00000566128.1:c.1212+89_1213-83del	ENSP00000456276.1:n.1212+89_1213-83del
NM_000078.2:c.1407+89_1408-83del	NP_000069.2:n.1407+89_1408-83del
NM_001286085.1:c.1227+89_1228-83del	NP_001273014.1:n.1227+89_1228-83del
NM_000078.3:c.1407+89_1408-83del MANE Select	NP_000069.2:n.1407+89_1408-83del
NM_001286085.2:c.1227+89_1228-83del	NP_001273014.1:n.1227+89_1228-83del