Canonical Allele Identifier: CA231279678

Gene: ACAD8

Linked Data

• dbSNP Id: rs1012128699
• gnomAD v3: 11-134262472-CCA-C
• gnomAD v4: 11-134262472-CCA-C
• MyVariant Identifiers: chr11:g.134132367_134132368del (hg19) ; chr11:g.134262473_134262474del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262475_134262476del , CM000673.2:g.134262475_134262476del	GRCh38
NC_000011.9:g.134132369_134132370del , CM000673.1:g.134132369_134132370del	GRCh37
NC_000011.8:g.133637579_133637580del	NCBI36
NG_015842.1:g.13936_13937del , LRG_448:g.13936_13937del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281182.9:c.1093-45_1093-44del MANE Select	ENSP00000281182.5:n.1093-45_1093-44del
ENST00000281182.8:c.1093-45_1093-44del	ENSP00000281182.4:n.1093-45_1093-44del
ENST00000374752.6:c.712-45_712-44del	ENSP00000363884.4:n.712-45_712-44del
ENST00000524426.5:c.*823-45_*823-44del	ENSP00000431310.1:n.*823-45_*823-44del
ENST00000524502.2:n.93-45_93-44del
ENST00000524547.5:n.696-45_696-44del
ENST00000526026.5:c.*782-45_*782-44del	ENSP00000431532.1:n.*782-45_*782-44del
ENST00000531338.5:n.1292_1293del
ENST00000533387.5:n.2152-45_2152-44del
NM_014384.2:c.1093-45_1093-44del , LRG_448t1:c.1093-45_1093-44del	NP_055199.1:n.1093-45_1093-44del
XM_005271501.2:c.1093-45_1093-44del	XP_005271558.1:n.1093-45_1093-44del
XM_011542750.1:c.1093-45_1093-44del	XP_011541052.1:n.1093-45_1093-44del
XR_947819.1:n.1157-45_1157-44del
XR_947820.1:n.1500_1501del
XR_947821.1:n.1302-45_1302-44del
XR_947822.1:n.987-45_987-44del
XR_947823.1:n.1143-45_1143-44del
XM_005271505.4:c.*1358-45_*1358-44del	XP_005271562.1:n.*1358-45_*1358-44del
XM_011542750.3:c.1093-45_1093-44del	XP_011541052.1:n.1093-45_1093-44del
XM_017017542.2:c.1093-45_1093-44del	XP_016873031.1:n.1093-45_1093-44del
XM_017017543.2:c.1093-45_1093-44del	XP_016873032.1:n.1093-45_1093-44del
XM_017017544.2:c.*62-45_*62-44del	XP_016873033.1:n.*62-45_*62-44del
XM_017017545.2:c.*260_*261del	XP_016873034.1:n.*260_*261del
XM_017017546.2:c.799-45_799-44del	XP_016873035.1:n.799-45_799-44del
XM_017017547.2:c.799-45_799-44del	XP_016873036.1:n.799-45_799-44del
XM_017017548.2:c.*1729-45_*1729-44del	XP_016873037.1:n.*1729-45_*1729-44del
XM_017017549.2:c.*1503-45_*1503-44del	XP_016873038.1:n.*1503-45_*1503-44del
XM_024448437.1:c.*195_*196del	XP_024304205.1:n.*195_*196del
XM_024448438.1:c.712-45_712-44del	XP_024304206.1:n.712-45_712-44del
NM_014384.3:c.1093-45_1093-44del MANE Select	NP_055199.1:n.1093-45_1093-44del