Canonical Allele Identifier: CA673792243

Gene: ACAD8

Linked Data

• dbSNP Id: rs1436431965
• MyVariant Identifiers: chr11:g.134132460_134132474del (hg19) ; chr11:g.134262566_134262580del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262568_134262582del , CM000673.2:g.134262568_134262582del	GRCh38
NC_000011.9:g.134132462_134132476del , CM000673.1:g.134132462_134132476del	GRCh37
NC_000011.8:g.133637672_133637686del	NCBI36
NG_015842.1:g.14029_14043del , LRG_448:g.14029_14043del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281182.9:c.1141_1155del MANE Select	ENSP00000281182.5:p.Asp381_Gln385del
ENST00000281182.8:c.1141_1155del	ENSP00000281182.4:p.Asp381_Gln385del
ENST00000374752.6:c.760_774del	ENSP00000363884.4:p.Asp254_Gln258del
ENST00000524426.5:c.*871_*885del	ENSP00000431310.1:n.*871_*885del
ENST00000524502.2:n.141_155del
ENST00000526026.5:c.*830_*844del	ENSP00000431532.1:n.*830_*844del
ENST00000531338.5:n.1385_1399del
ENST00000533387.5:n.2200_2214del
NM_014384.2:c.1141_1155del , LRG_448t1:c.1141_1155del	NP_055199.1:p.Asp381_Gln385del
XM_005271501.2:c.1141_1155del	XP_005271558.1:p.Asp381_Gln385del
XM_011542750.1:c.1141_1155del	XP_011541052.1:p.Asp381_Gln385del
XR_947819.1:n.1205_1219del
XR_947820.1:n.1593_1607del
XR_947821.1:n.1350_1364del
XR_947822.1:n.1035_1049del
XR_947823.1:n.1191_1205del
XM_005271505.4:c.*1406_*1420del	XP_005271562.1:n.*1406_*1420del
XM_011542750.3:c.1141_1155del	XP_011541052.1:p.Asp381_Gln385del
XM_017017542.2:c.1141_1155del	XP_016873031.1:p.Asp381_Gln385del
XM_017017543.2:c.1141_1155del	XP_016873032.1:p.Asp381_Gln385del
XM_017017544.2:c.*110_*124del	XP_016873033.1:n.*110_*124del
XM_017017545.2:c.*353_*367del	XP_016873034.1:n.*353_*367del
XM_017017546.2:c.847_861del	XP_016873035.1:p.Asp283_Gln287del
XM_017017547.2:c.847_861del	XP_016873036.1:p.Asp283_Gln287del
XM_017017548.2:c.*1777_*1791del	XP_016873037.1:n.*1777_*1791del
XM_017017549.2:c.*1551_*1565del	XP_016873038.1:n.*1551_*1565del
XM_024448437.1:c.*288_*302del	XP_024304205.1:n.*288_*302del
XM_024448438.1:c.760_774del	XP_024304206.1:p.Asp254_Gln258del
NM_014384.3:c.1141_1155del MANE Select	NP_055199.1:p.Asp381_Gln385del