Canonical Allele Identifier: CA2245712477
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223981A= , CM000679.2:g.7223981A= GRCh38
NC_000017.10:g.7127300A= , CM000679.1:g.7127300A= GRCh37
NC_000017.9:g.7068024A= NCBI36
NG_007975.1:g.9148A=
NG_008391.2:g.1070T=
NG_033038.1:g.15564T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1346A= MANE Select ENSP00000349297.5:p.Glu449=
ENST00000322910.9:c.*1301A= ENSP00000325395.5:n.*1301A=
ENST00000350303.9:c.1280A= ENSP00000344152.5:p.Glu427=
ENST00000356839.9:c.1346A= ENSP00000349297.5:p.Glu449=
ENST00000542255.6:c.204A=
ENST00000543245.6:c.1415A= ENSP00000438689.2:p.Glu472=
ENST00000578711.1:n.477A=
ENST00000579425.5:n.462A=
ENST00000579546.1:c.183A=
ENST00000579894.5:n.57A=
ENST00000583074.5:n.65A=
ENST00000583850.5:n.121A=
ENST00000583858.5:c.375A=
ENST00000585203.6:n.537A=
NM_000018.3:c.1346A= NP_000009.1:p.Glu449=
NM_001033859.2:c.1280A= NP_001029031.1:p.Glu427=
NM_001270447.1:c.1415A= NP_001257376.1:p.Glu472=
NM_001270448.1:c.1118A= NP_001257377.1:p.Glu373=
XM_006721516.2:c.1346A= XP_006721579.2:p.Glu449=
XM_011523829.1:c.1346A= XP_011522131.1:p.Glu449=
XM_011523830.1:c.1346A= XP_011522132.1:p.Glu449=
XR_934021.1:n.1453A=
XR_934022.1:n.1453A=
XR_934023.1:n.1453A=
XM_006721516.3:c.1346A= XP_006721579.2:p.Glu449=
XM_011523829.2:c.1346A= XP_011522131.1:p.Glu449=
XM_011523830.2:c.1346A= XP_011522132.1:p.Glu449=
XM_024450741.1:c.1346A= XP_024306509.1:p.Glu449=
XR_934021.2:n.1405A=
XR_934022.2:n.1405A=
XR_934023.2:n.1405A=
NM_000018.4:c.1346A= MANE Select NP_000009.1:p.Glu449=
NM_001033859.3:c.1280A= NP_001029031.1:p.Glu427=
NM_001270447.2:c.1415A= NP_001257376.1:p.Glu472=
NM_001270448.2:c.1118A= NP_001257377.1:p.Glu373=