Canonical Allele Identifier: CA2245714518
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224517A= , CM000679.2:g.7224517A= GRCh38
NC_000017.10:g.7127836A= , CM000679.1:g.7127836A= GRCh37
NC_000017.9:g.7068560A= NCBI36
NG_007975.1:g.9684A=
NG_008391.2:g.534T=
NG_033038.1:g.15028T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1643A= MANE Select ENSP00000349297.5:p.Glu548=
ENST00000322910.9:c.*1598A= ENSP00000325395.5:n.*1598A=
ENST00000350303.9:c.1577A= ENSP00000344152.5:p.Glu526=
ENST00000356839.9:c.1643A= ENSP00000349297.5:p.Glu548=
ENST00000542255.6:c.501A=
ENST00000543245.6:c.1712A= ENSP00000438689.2:p.Glu571=
ENST00000578319.5:n.224A=
ENST00000578711.1:n.1013A=
ENST00000578809.5:n.215A=
ENST00000579391.1:n.247A=
ENST00000579425.5:n.759A=
ENST00000579546.1:c.378A=
ENST00000582450.1:n.151A=
ENST00000583074.5:n.264A=
ENST00000583848.5:c.29A= ENSP00000466487.1:p.Glu10=
ENST00000583850.5:n.414A=
ENST00000583858.5:c.574A=
ENST00000585203.6:n.834A=
NM_000018.3:c.1643A= NP_000009.1:p.Glu548=
NM_001033859.2:c.1577A= NP_001029031.1:p.Glu526=
NM_001270447.1:c.1712A= NP_001257376.1:p.Glu571=
NM_001270448.1:c.1415A= NP_001257377.1:p.Glu472=
XM_006721516.2:c.1643A= XP_006721579.2:p.Glu548=
XM_011523829.1:c.1541A= XP_011522131.1:p.Glu514=
XM_011523830.1:c.1541A= XP_011522132.1:p.Glu514=
XR_934021.1:n.1746A=
XR_934022.1:n.1652A=
XR_934023.1:n.1652A=
XM_006721516.3:c.1643A= XP_006721579.2:p.Glu548=
XM_011523829.2:c.1541A= XP_011522131.1:p.Glu514=
XM_011523830.2:c.1541A= XP_011522132.1:p.Glu514=
XM_024450741.1:c.1631A= XP_024306509.1:p.Glu544=
XR_934021.2:n.1698A=
XR_934022.2:n.1604A=
XR_934023.2:n.1604A=
NM_000018.4:c.1643A= MANE Select NP_000009.1:p.Glu548=
NM_001033859.3:c.1577A= NP_001029031.1:p.Glu526=
NM_001270447.2:c.1712A= NP_001257376.1:p.Glu571=
NM_001270448.2:c.1415A= NP_001257377.1:p.Glu472=