Canonical Allele Identifier: CA2245716452
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225060G= , CM000679.2:g.7225060G= GRCh38
NC_000017.10:g.7128379G= , CM000679.1:g.7128379G= GRCh37
NC_000017.9:g.7069103G= NCBI36
NG_007975.1:g.10227G=
NG_033038.1:g.14485C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1931G= MANE Select ENSP00000349297.5:p.Arg644=
ENST00000322910.9:c.*1886G= ENSP00000325395.5:n.*1886G=
ENST00000350303.9:c.1865G= ENSP00000344152.5:p.Arg622=
ENST00000356839.9:c.1931G= ENSP00000349297.5:p.Arg644=
ENST00000542255.6:c.810G=
ENST00000543245.6:c.2000G= ENSP00000438689.2:p.Arg667=
ENST00000578033.1:n.356G=
ENST00000578319.5:n.512G=
ENST00000578711.1:n.1556G=
ENST00000578809.5:n.503G=
ENST00000579425.5:n.1047G=
ENST00000583848.5:c.297G= ENSP00000466487.1:n.297G=
ENST00000583850.5:n.702G=
ENST00000583858.5:c.862G=
NM_000018.3:c.1931G= NP_000009.1:p.Arg644=
NM_001033859.2:c.1865G= NP_001029031.1:p.Arg622=
NM_001270447.1:c.2000G= NP_001257376.1:p.Arg667=
NM_001270448.1:c.1703G= NP_001257377.1:p.Arg568=
XM_006721516.2:c.1952G= XP_006721579.2:p.Arg651=
XM_011523829.1:c.1850G= XP_011522131.1:p.Arg617=
XM_011523830.1:c.1829G= XP_011522132.1:p.Arg610=
XR_934021.1:n.2034G=
XR_934022.1:n.1940G=
XR_934023.1:n.1961G=
XM_006721516.3:c.1952G= XP_006721579.2:p.Arg651=
XM_011523829.2:c.1850G= XP_011522131.1:p.Arg617=
XM_011523830.2:c.1829G= XP_011522132.1:p.Arg610=
XM_024450741.1:c.1919G= XP_024306509.1:p.Arg640=
XR_934021.2:n.1986G=
XR_934022.2:n.1892G=
XR_934023.2:n.1913G=
NM_000018.4:c.1931G= MANE Select NP_000009.1:p.Arg644=
NM_001033859.3:c.1865G= NP_001029031.1:p.Arg622=
NM_001270447.2:c.2000G= NP_001257376.1:p.Arg667=
NM_001270448.2:c.1703G= NP_001257377.1:p.Arg568=