Canonical Allele Identifier: CA3047141823

Gene: CETP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56982179_56982180delinsAA , CM000678.2:g.56982179_56982180delinsAA	GRCh38
NC_000016.9:g.57016091_57016092delinsAA , CM000678.1:g.57016091_57016092delinsAA	GRCh37
NC_000016.8:g.55573592_55573593delinsAA	NCBI36
NG_008952.1:g.25257_25258delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1263_1264delinsAA MANE Select	ENSP00000200676.3:p.Val422Ile
ENST00000650358.1:n.1661_1662delinsAA
ENST00000200676.7:c.1263_1264delinsAA	ENSP00000200676.3:p.Val422Ile
ENST00000379780.6:c.1083_1084delinsAA	ENSP00000369106.2:p.Val362Ile
ENST00000566128.1:c.1068_1069delinsAA	ENSP00000456276.1:p.Val357Ile
NM_000078.2:c.1263_1264delinsAA	NP_000069.2:p.Val422Ile
NM_001286085.1:c.1083_1084delinsAA	NP_001273014.1:p.Val362Ile
NM_000078.3:c.1263_1264delinsAA MANE Select	NP_000069.2:p.Val422Ile
NM_001286085.2:c.1083_1084delinsAA	NP_001273014.1:p.Val362Ile