Canonical Allele Identifier: CA2245713426
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224223G= , CM000679.2:g.7224223G= GRCh38
NC_000017.10:g.7127542G= , CM000679.1:g.7127542G= GRCh37
NC_000017.9:g.7068266G= NCBI36
NG_007975.1:g.9390G=
NG_008391.2:g.828C=
NG_033038.1:g.15322C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1512G= MANE Select ENSP00000349297.5:p.Glu504=
ENST00000322910.9:c.*1467G= ENSP00000325395.5:n.*1467G=
ENST00000350303.9:c.1446G= ENSP00000344152.5:p.Glu482=
ENST00000356839.9:c.1512G= ENSP00000349297.5:p.Glu504=
ENST00000542255.6:c.370G=
ENST00000543245.6:c.1581G= ENSP00000438689.2:p.Glu527=
ENST00000578319.5:n.7G=
ENST00000578711.1:n.719G=
ENST00000578809.5:n.7G=
ENST00000579391.1:n.120G=
ENST00000579425.5:n.628G=
ENST00000579546.1:c.272-98G=
ENST00000579894.5:n.299G=
ENST00000583074.5:n.154-98G=
ENST00000583850.5:n.287G=
ENST00000583858.5:c.464-98G=
ENST00000585203.6:n.703G=
NM_000018.3:c.1512G= NP_000009.1:p.Glu504=
NM_001033859.2:c.1446G= NP_001029031.1:p.Glu482=
NM_001270447.1:c.1581G= NP_001257376.1:p.Glu527=
NM_001270448.1:c.1284G= NP_001257377.1:p.Glu428=
XM_006721516.2:c.1512G= XP_006721579.2:p.Glu504=
XM_011523829.1:c.1435-98G= XP_011522131.1:n.1435-98G=
XM_011523830.1:c.1435-98G= XP_011522132.1:n.1435-98G=
XR_934021.1:n.1619G=
XR_934022.1:n.1542-98G=
XR_934023.1:n.1542-98G=
XM_006721516.3:c.1512G= XP_006721579.2:p.Glu504=
XM_011523829.2:c.1435-98G= XP_011522131.1:n.1435-98G=
XM_011523830.2:c.1435-98G= XP_011522132.1:n.1435-98G=
XM_024450741.1:c.1435-98G= XP_024306509.1:n.1435-98G=
XR_934021.2:n.1571G=
XR_934022.2:n.1494-98G=
XR_934023.2:n.1494-98G=
NM_000018.4:c.1512G= MANE Select NP_000009.1:p.Glu504=
NM_001033859.3:c.1446G= NP_001029031.1:p.Glu482=
NM_001270447.2:c.1581G= NP_001257376.1:p.Glu527=
NM_001270448.2:c.1284G= NP_001257377.1:p.Glu428=