Canonical Allele Identifier: CA383519310
Gene: ACAD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134262595G>A , CM000673.2:g.134262595G>A GRCh38
NC_000011.9:g.134132489G>A , CM000673.1:g.134132489G>A GRCh37
NC_000011.8:g.133637699G>A NCBI36
NG_015842.1:g.14056G>A , LRG_448:g.14056G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281182.9:c.1168G>A MANE Select ENSP00000281182.5:p.Asp390Asn
ENST00000281182.8:c.1168G>A ENSP00000281182.4:p.Asp390Asn
ENST00000374752.6:c.787G>A ENSP00000363884.4:p.Asp263Asn
ENST00000524426.5:c.*898G>A ENSP00000431310.1:n.*898G>A
ENST00000524502.2:n.168G>A
ENST00000526026.5:c.*857G>A ENSP00000431532.1:n.*857G>A
ENST00000531338.5:n.1412G>A
ENST00000533387.5:n.2227G>A
NM_014384.2:c.1168G>A , LRG_448t1:c.1168G>A NP_055199.1:p.Asp390Asn
XM_005271501.2:c.1168G>A XP_005271558.1:p.Asp390Asn
XM_011542750.1:c.1168G>A XP_011541052.1:p.Asp390Asn
XR_947819.1:n.1232G>A
XR_947820.1:n.1620G>A
XR_947821.1:n.1377G>A
XR_947822.1:n.1062G>A
XR_947823.1:n.1218G>A
XM_005271505.4:c.*1433G>A XP_005271562.1:n.*1433G>A
XM_011542750.3:c.1168G>A XP_011541052.1:p.Asp390Asn
XM_017017542.2:c.1168G>A XP_016873031.1:p.Asp390Asn
XM_017017543.2:c.1168G>A XP_016873032.1:p.Asp390Asn
XM_017017544.2:c.*137G>A XP_016873033.1:n.*137G>A
XM_017017545.2:c.*380G>A XP_016873034.1:n.*380G>A
XM_017017546.2:c.874G>A XP_016873035.1:p.Asp292Asn
XM_017017547.2:c.874G>A XP_016873036.1:p.Asp292Asn
XM_017017548.2:c.*1804G>A XP_016873037.1:n.*1804G>A
XM_017017549.2:c.*1578G>A XP_016873038.1:n.*1578G>A
XM_024448437.1:c.*315G>A XP_024304205.1:n.*315G>A
XM_024448438.1:c.787G>A XP_024304206.1:p.Asp263Asn
NM_014384.3:c.1168G>A MANE Select NP_055199.1:p.Asp390Asn