Canonical Allele Identifier: CA2245715118
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224673C= , CM000679.2:g.7224673C= GRCh38
NC_000017.10:g.7127992C= , CM000679.1:g.7127992C= GRCh37
NC_000017.9:g.7068716C= NCBI36
NG_007975.1:g.9840C=
NG_008391.2:g.378G=
NG_033038.1:g.14872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1710C= MANE Select ENSP00000349297.5:p.Asp570=
ENST00000322910.9:c.*1665C= ENSP00000325395.5:n.*1665C=
ENST00000350303.9:c.1644C= ENSP00000344152.5:p.Asp548=
ENST00000356839.9:c.1710C= ENSP00000349297.5:p.Asp570=
ENST00000542255.6:c.537-42C=
ENST00000543245.6:c.1779C= ENSP00000438689.2:p.Asp593=
ENST00000578033.1:n.41C=
ENST00000578319.5:n.291C=
ENST00000578711.1:n.1169C=
ENST00000578809.5:n.282C=
ENST00000579425.5:n.826C=
ENST00000579546.1:c.445C=
ENST00000583074.5:n.300-42C=
ENST00000583848.5:c.76C= ENSP00000466487.1:p.Arg26=
ENST00000583850.5:n.481C=
ENST00000583858.5:c.641C=
ENST00000585203.6:n.901C=
NM_000018.3:c.1710C= NP_000009.1:p.Asp570=
NM_001033859.2:c.1644C= NP_001029031.1:p.Asp548=
NM_001270447.1:c.1779C= NP_001257376.1:p.Asp593=
NM_001270448.1:c.1482C= NP_001257377.1:p.Asp494=
XM_006721516.2:c.1679-42C= XP_006721579.2:n.1679-42C=
XM_011523829.1:c.1577-42C= XP_011522131.1:n.1577-42C=
XM_011523830.1:c.1608C= XP_011522132.1:p.Asp536=
XR_934021.1:n.1813C=
XR_934022.1:n.1719C=
XR_934023.1:n.1688-42C=
XM_006721516.3:c.1679-42C= XP_006721579.2:n.1679-42C=
XM_011523829.2:c.1577-42C= XP_011522131.1:n.1577-42C=
XM_011523830.2:c.1608C= XP_011522132.1:p.Asp536=
XM_024450741.1:c.1698C= XP_024306509.1:p.Asp566=
XR_934021.2:n.1765C=
XR_934022.2:n.1671C=
XR_934023.2:n.1640-42C=
NM_000018.4:c.1710C= MANE Select NP_000009.1:p.Asp570=
NM_001033859.3:c.1644C= NP_001029031.1:p.Asp548=
NM_001270447.2:c.1779C= NP_001257376.1:p.Asp593=
NM_001270448.2:c.1482C= NP_001257377.1:p.Asp494=