Canonical Allele Identifier: CA943830240

Gene: ACAD8

Linked Data

• dbSNP Id: rs1939979464
• gnomAD v3: 11-134262887-TAATG-T
• gnomAD v4: 11-134262887-TAATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262888_134262891del , CM000673.2:g.134262888_134262891del	GRCh38
NC_000011.9:g.134132782_134132785del , CM000673.1:g.134132782_134132785del	GRCh37
NC_000011.8:g.133637992_133637995del	NCBI36
NG_015842.1:g.14349_14352del , LRG_448:g.14349_14352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+266_1195+269del MANE Select	ENSP00000281182.5:n.1195+266_1195+269del
ENST00000281182.8:c.1195+266_1195+269del	ENSP00000281182.4:n.1195+266_1195+269del
ENST00000374752.6:c.814+266_814+269del	ENSP00000363884.4:n.814+266_814+269del
ENST00000524502.2:n.314_317del
ENST00000526026.5:c.*1003_*1006del	ENSP00000431532.1:n.*1003_*1006del
ENST00000531338.5:n.1705_1708del
ENST00000533387.5:n.2254+266_2254+269del
NM_014384.2:c.1195+266_1195+269del , LRG_448t1:c.1195+266_1195+269del	NP_055199.1:n.1195+266_1195+269del
XM_005271501.2:c.*9_*12del	XP_005271558.1:n.*9_*12del
XM_011542750.1:c.1195+266_1195+269del	XP_011541052.1:n.1195+266_1195+269del
XR_947819.1:n.1259+266_1259+269del
XR_947820.1:n.1913_1916del
XR_947822.1:n.1089+266_1089+269del
XR_947823.1:n.1245+266_1245+269del
XM_005271505.4:c.*1460+266_*1460+269del	XP_005271562.1:n.*1460+266_*1460+269del
XM_011542750.3:c.1195+266_1195+269del	XP_011541052.1:n.1195+266_1195+269del
XM_017017542.2:c.1195+266_1195+269del	XP_016873031.1:n.1195+266_1195+269del
XM_017017543.2:c.*9_*12del	XP_016873032.1:n.*9_*12del
XM_017017544.2:c.*164+266_*164+269del	XP_016873033.1:n.*164+266_*164+269del
XM_017017545.2:c.*673_*676del	XP_016873034.1:n.*673_*676del
XM_017017546.2:c.901+266_901+269del	XP_016873035.1:n.901+266_901+269del
XM_017017547.2:c.901+266_901+269del	XP_016873036.1:n.901+266_901+269del
XM_017017548.2:c.*1950_*1953del	XP_016873037.1:n.*1950_*1953del
XM_017017549.2:c.*1605+266_*1605+269del	XP_016873038.1:n.*1605+266_*1605+269del
XM_024448437.1:c.*608_*611del	XP_024304205.1:n.*608_*611del
XM_024448438.1:c.814+266_814+269del	XP_024304206.1:n.814+266_814+269del
NM_014384.3:c.1195+266_1195+269del MANE Select	NP_055199.1:n.1195+266_1195+269del