Canonical Allele Identifier: CA2245714522
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224518G= , CM000679.2:g.7224518G= GRCh38
NC_000017.10:g.7127837G= , CM000679.1:g.7127837G= GRCh37
NC_000017.9:g.7068561G= NCBI36
NG_007975.1:g.9685G=
NG_008391.2:g.533C=
NG_033038.1:g.15027C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1644G= MANE Select ENSP00000349297.5:p.Glu548=
ENST00000322910.9:c.*1599G= ENSP00000325395.5:n.*1599G=
ENST00000350303.9:c.1578G= ENSP00000344152.5:p.Glu526=
ENST00000356839.9:c.1644G= ENSP00000349297.5:p.Glu548=
ENST00000542255.6:c.502G=
ENST00000543245.6:c.1713G= ENSP00000438689.2:p.Glu571=
ENST00000578319.5:n.225G=
ENST00000578711.1:n.1014G=
ENST00000578809.5:n.216G=
ENST00000579391.1:n.248G=
ENST00000579425.5:n.760G=
ENST00000579546.1:c.379G=
ENST00000582450.1:n.152G=
ENST00000583074.5:n.265G=
ENST00000583848.5:c.30G= ENSP00000466487.1:p.Glu10=
ENST00000583850.5:n.415G=
ENST00000583858.5:c.575G=
ENST00000585203.6:n.835G=
NM_000018.3:c.1644G= NP_000009.1:p.Glu548=
NM_001033859.2:c.1578G= NP_001029031.1:p.Glu526=
NM_001270447.1:c.1713G= NP_001257376.1:p.Glu571=
NM_001270448.1:c.1416G= NP_001257377.1:p.Glu472=
XM_006721516.2:c.1644G= XP_006721579.2:p.Glu548=
XM_011523829.1:c.1542G= XP_011522131.1:p.Glu514=
XM_011523830.1:c.1542G= XP_011522132.1:p.Glu514=
XR_934021.1:n.1747G=
XR_934022.1:n.1653G=
XR_934023.1:n.1653G=
XM_006721516.3:c.1644G= XP_006721579.2:p.Glu548=
XM_011523829.2:c.1542G= XP_011522131.1:p.Glu514=
XM_011523830.2:c.1542G= XP_011522132.1:p.Glu514=
XM_024450741.1:c.1632G= XP_024306509.1:p.Glu544=
XR_934021.2:n.1699G=
XR_934022.2:n.1605G=
XR_934023.2:n.1605G=
NM_000018.4:c.1644G= MANE Select NP_000009.1:p.Glu548=
NM_001033859.3:c.1578G= NP_001029031.1:p.Glu526=
NM_001270447.2:c.1713G= NP_001257376.1:p.Glu571=
NM_001270448.2:c.1416G= NP_001257377.1:p.Glu472=