Canonical Allele Identifier: CA2245713439
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224226A= , CM000679.2:g.7224226A= GRCh38
NC_000017.10:g.7127545A= , CM000679.1:g.7127545A= GRCh37
NC_000017.9:g.7068269A= NCBI36
NG_007975.1:g.9393A=
NG_008391.2:g.825T=
NG_033038.1:g.15319T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1515A= MANE Select ENSP00000349297.5:p.Ala505=
ENST00000322910.9:c.*1470A= ENSP00000325395.5:n.*1470A=
ENST00000350303.9:c.1449A= ENSP00000344152.5:p.Ala483=
ENST00000356839.9:c.1515A= ENSP00000349297.5:p.Ala505=
ENST00000542255.6:c.373A=
ENST00000543245.6:c.1584A= ENSP00000438689.2:p.Ala528=
ENST00000578319.5:n.10A=
ENST00000578711.1:n.722A=
ENST00000578809.5:n.10A=
ENST00000579391.1:n.123A=
ENST00000579425.5:n.631A=
ENST00000579546.1:c.272-95A=
ENST00000579894.5:n.302A=
ENST00000583074.5:n.154-95A=
ENST00000583850.5:n.290A=
ENST00000583858.5:c.464-95A=
ENST00000585203.6:n.706A=
NM_000018.3:c.1515A= NP_000009.1:p.Ala505=
NM_001033859.2:c.1449A= NP_001029031.1:p.Ala483=
NM_001270447.1:c.1584A= NP_001257376.1:p.Ala528=
NM_001270448.1:c.1287A= NP_001257377.1:p.Ala429=
XM_006721516.2:c.1515A= XP_006721579.2:p.Ala505=
XM_011523829.1:c.1435-95A= XP_011522131.1:n.1435-95A=
XM_011523830.1:c.1435-95A= XP_011522132.1:n.1435-95A=
XR_934021.1:n.1622A=
XR_934022.1:n.1542-95A=
XR_934023.1:n.1542-95A=
XM_006721516.3:c.1515A= XP_006721579.2:p.Ala505=
XM_011523829.2:c.1435-95A= XP_011522131.1:n.1435-95A=
XM_011523830.2:c.1435-95A= XP_011522132.1:n.1435-95A=
XM_024450741.1:c.1435-95A= XP_024306509.1:n.1435-95A=
XR_934021.2:n.1574A=
XR_934022.2:n.1494-95A=
XR_934023.2:n.1494-95A=
NM_000018.4:c.1515A= MANE Select NP_000009.1:p.Ala505=
NM_001033859.3:c.1449A= NP_001029031.1:p.Ala483=
NM_001270447.2:c.1584A= NP_001257376.1:p.Ala528=
NM_001270448.2:c.1287A= NP_001257377.1:p.Ala429=