Canonical Allele Identifier: CA2245716435
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225058G= , CM000679.2:g.7225058G= GRCh38
NC_000017.10:g.7128377G= , CM000679.1:g.7128377G= GRCh37
NC_000017.9:g.7069101G= NCBI36
NG_007975.1:g.10225G=
NG_033038.1:g.14487C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1929G= MANE Select ENSP00000349297.5:p.Glu643=
ENST00000322910.9:c.*1884G= ENSP00000325395.5:n.*1884G=
ENST00000350303.9:c.1863G= ENSP00000344152.5:p.Glu621=
ENST00000356839.9:c.1929G= ENSP00000349297.5:p.Glu643=
ENST00000542255.6:c.808G=
ENST00000543245.6:c.1998G= ENSP00000438689.2:p.Glu666=
ENST00000578033.1:n.354G=
ENST00000578319.5:n.510G=
ENST00000578711.1:n.1554G=
ENST00000578809.5:n.501G=
ENST00000579425.5:n.1045G=
ENST00000583848.5:c.295G= ENSP00000466487.1:n.295G=
ENST00000583850.5:n.700G=
ENST00000583858.5:c.860G=
NM_000018.3:c.1929G= NP_000009.1:p.Glu643=
NM_001033859.2:c.1863G= NP_001029031.1:p.Glu621=
NM_001270447.1:c.1998G= NP_001257376.1:p.Glu666=
NM_001270448.1:c.1701G= NP_001257377.1:p.Glu567=
XM_006721516.2:c.1950G= XP_006721579.2:p.Glu650=
XM_011523829.1:c.1848G= XP_011522131.1:p.Glu616=
XM_011523830.1:c.1827G= XP_011522132.1:p.Glu609=
XR_934021.1:n.2032G=
XR_934022.1:n.1938G=
XR_934023.1:n.1959G=
XM_006721516.3:c.1950G= XP_006721579.2:p.Glu650=
XM_011523829.2:c.1848G= XP_011522131.1:p.Glu616=
XM_011523830.2:c.1827G= XP_011522132.1:p.Glu609=
XM_024450741.1:c.1917G= XP_024306509.1:p.Glu639=
XR_934021.2:n.1984G=
XR_934022.2:n.1890G=
XR_934023.2:n.1911G=
NM_000018.4:c.1929G= MANE Select NP_000009.1:p.Glu643=
NM_001033859.3:c.1863G= NP_001029031.1:p.Glu621=
NM_001270447.2:c.1998G= NP_001257376.1:p.Glu666=
NM_001270448.2:c.1701G= NP_001257377.1:p.Glu567=