Canonical Allele Identifier: CA2245713416
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224221G= , CM000679.2:g.7224221G= GRCh38
NC_000017.10:g.7127540G= , CM000679.1:g.7127540G= GRCh37
NC_000017.9:g.7068264G= NCBI36
NG_007975.1:g.9388G=
NG_008391.2:g.830C=
NG_033038.1:g.15324C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1510G= MANE Select ENSP00000349297.5:p.Glu504=
ENST00000322910.9:c.*1465G= ENSP00000325395.5:n.*1465G=
ENST00000350303.9:c.1444G= ENSP00000344152.5:p.Glu482=
ENST00000356839.9:c.1510G= ENSP00000349297.5:p.Glu504=
ENST00000542255.6:c.368G=
ENST00000543245.6:c.1579G= ENSP00000438689.2:p.Glu527=
ENST00000578319.5:n.5G=
ENST00000578711.1:n.717G=
ENST00000578809.5:n.5G=
ENST00000579391.1:n.118G=
ENST00000579425.5:n.626G=
ENST00000579546.1:c.272-100G=
ENST00000579894.5:n.297G=
ENST00000583074.5:n.154-100G=
ENST00000583850.5:n.285G=
ENST00000583858.5:c.464-100G=
ENST00000585203.6:n.701G=
NM_000018.3:c.1510G= NP_000009.1:p.Glu504=
NM_001033859.2:c.1444G= NP_001029031.1:p.Glu482=
NM_001270447.1:c.1579G= NP_001257376.1:p.Glu527=
NM_001270448.1:c.1282G= NP_001257377.1:p.Glu428=
XM_006721516.2:c.1510G= XP_006721579.2:p.Glu504=
XM_011523829.1:c.1435-100G= XP_011522131.1:n.1435-100G=
XM_011523830.1:c.1435-100G= XP_011522132.1:n.1435-100G=
XR_934021.1:n.1617G=
XR_934022.1:n.1542-100G=
XR_934023.1:n.1542-100G=
XM_006721516.3:c.1510G= XP_006721579.2:p.Glu504=
XM_011523829.2:c.1435-100G= XP_011522131.1:n.1435-100G=
XM_011523830.2:c.1435-100G= XP_011522132.1:n.1435-100G=
XM_024450741.1:c.1435-100G= XP_024306509.1:n.1435-100G=
XR_934021.2:n.1569G=
XR_934022.2:n.1494-100G=
XR_934023.2:n.1494-100G=
NM_000018.4:c.1510G= MANE Select NP_000009.1:p.Glu504=
NM_001033859.3:c.1444G= NP_001029031.1:p.Glu482=
NM_001270447.2:c.1579G= NP_001257376.1:p.Glu527=
NM_001270448.2:c.1282G= NP_001257377.1:p.Glu428=