Canonical Allele Identifier: CA977671264

Gene: CETP

Linked Data

• dbSNP Id: rs2056087001
• gnomAD v3: 16-56968820-T-TTG
• gnomAD v4: 16-56968820-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968821_56968822insGT , CM000678.2:g.56968821_56968822insGT	GRCh38
NC_000016.9:g.57002733_57002734insGT , CM000678.1:g.57002733_57002734insGT	GRCh37
NC_000016.8:g.55560234_55560235insGT	NCBI36
NG_008952.1:g.11899_11900insGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-565_234-564insGT MANE Select	ENSP00000200676.3:n.234-565_234-564insGT
ENST00000200676.7:c.234-565_234-564insGT	ENSP00000200676.3:n.234-565_234-564insGT
ENST00000379780.6:c.234-565_234-564insGT	ENSP00000369106.2:n.234-565_234-564insGT
ENST00000566128.1:c.39-565_39-564insGT	ENSP00000456276.1:n.39-565_39-564insGT
ENST00000569082.1:n.232-565_232-564insGT
NM_000078.2:c.234-565_234-564insGT	NP_000069.2:n.234-565_234-564insGT
NM_001286085.1:c.234-565_234-564insGT	NP_001273014.1:n.234-565_234-564insGT
XM_006721124.2:c.234-565_234-564insGT	XP_006721187.1:n.234-565_234-564insGT
XM_006721124.3:c.234-565_234-564insGT	XP_006721187.1:n.234-565_234-564insGT
NM_000078.3:c.234-565_234-564insGT MANE Select	NP_000069.2:n.234-565_234-564insGT
NM_001286085.2:c.234-565_234-564insGT	NP_001273014.1:n.234-565_234-564insGT