Canonical Allele Identifier: CA622341176

Gene: CETP

Linked Data

• dbSNP Id: rs1368550094
• gnomAD v2: 16-57002638-CTTCTT-C
• gnomAD v3: 16-56968726-CTTCTT-C
• gnomAD v4: 16-56968726-CTTCTT-C
• MyVariant Identifiers: chr16:g.57002639_57002643del (hg19) ; chr16:g.56968727_56968731del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968729_56968733del , CM000678.2:g.56968729_56968733del	GRCh38
NC_000016.9:g.57002641_57002645del , CM000678.1:g.57002641_57002645del	GRCh37
NC_000016.8:g.55560142_55560146del	NCBI36
NG_008952.1:g.11807_11811del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-657_234-653del MANE Select	ENSP00000200676.3:n.234-657_234-653del
ENST00000200676.7:c.234-657_234-653del	ENSP00000200676.3:n.234-657_234-653del
ENST00000379780.6:c.234-657_234-653del	ENSP00000369106.2:n.234-657_234-653del
ENST00000566128.1:c.39-657_39-653del	ENSP00000456276.1:n.39-657_39-653del
ENST00000569082.1:n.232-657_232-653del
NM_000078.2:c.234-657_234-653del	NP_000069.2:n.234-657_234-653del
NM_001286085.1:c.234-657_234-653del	NP_001273014.1:n.234-657_234-653del
XM_006721124.2:c.234-657_234-653del	XP_006721187.1:n.234-657_234-653del
XM_006721124.3:c.234-657_234-653del	XP_006721187.1:n.234-657_234-653del
NM_000078.3:c.234-657_234-653del MANE Select	NP_000069.2:n.234-657_234-653del
NM_001286085.2:c.234-657_234-653del	NP_001273014.1:n.234-657_234-653del