Canonical Allele Identifier: CA383519155
Gene: ACAD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134262565A>G , CM000673.2:g.134262565A>G GRCh38
NC_000011.9:g.134132459A>G , CM000673.1:g.134132459A>G GRCh37
NC_000011.8:g.133637669A>G NCBI36
NG_015842.1:g.14026A>G , LRG_448:g.14026A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281182.9:c.1138A>G MANE Select ENSP00000281182.5:p.Lys380Glu
ENST00000281182.8:c.1138A>G ENSP00000281182.4:p.Lys380Glu
ENST00000374752.6:c.757A>G ENSP00000363884.4:p.Lys253Glu
ENST00000524426.5:c.*868A>G ENSP00000431310.1:n.*868A>G
ENST00000524502.2:n.138A>G
ENST00000526026.5:c.*827A>G ENSP00000431532.1:n.*827A>G
ENST00000531338.5:n.1382A>G
ENST00000533387.5:n.2197A>G
NM_014384.2:c.1138A>G , LRG_448t1:c.1138A>G NP_055199.1:p.Lys380Glu
XM_005271501.2:c.1138A>G XP_005271558.1:p.Lys380Glu
XM_011542750.1:c.1138A>G XP_011541052.1:p.Lys380Glu
XR_947819.1:n.1202A>G
XR_947820.1:n.1590A>G
XR_947821.1:n.1347A>G
XR_947822.1:n.1032A>G
XR_947823.1:n.1188A>G
XM_005271505.4:c.*1403A>G XP_005271562.1:n.*1403A>G
XM_011542750.3:c.1138A>G XP_011541052.1:p.Lys380Glu
XM_017017542.2:c.1138A>G XP_016873031.1:p.Lys380Glu
XM_017017543.2:c.1138A>G XP_016873032.1:p.Lys380Glu
XM_017017544.2:c.*107A>G XP_016873033.1:n.*107A>G
XM_017017545.2:c.*350A>G XP_016873034.1:n.*350A>G
XM_017017546.2:c.844A>G XP_016873035.1:p.Lys282Glu
XM_017017547.2:c.844A>G XP_016873036.1:p.Lys282Glu
XM_017017548.2:c.*1774A>G XP_016873037.1:n.*1774A>G
XM_017017549.2:c.*1548A>G XP_016873038.1:n.*1548A>G
XM_024448437.1:c.*285A>G XP_024304205.1:n.*285A>G
XM_024448438.1:c.757A>G XP_024304206.1:p.Lys253Glu
NM_014384.3:c.1138A>G MANE Select NP_055199.1:p.Lys380Glu