Canonical Allele Identifier: CA2245716457
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225061G= , CM000679.2:g.7225061G= GRCh38
NC_000017.10:g.7128380G= , CM000679.1:g.7128380G= GRCh37
NC_000017.9:g.7069104G= NCBI36
NG_007975.1:g.10228G=
NG_033038.1:g.14484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1932G= MANE Select ENSP00000349297.5:p.Arg644=
ENST00000322910.9:c.*1887G= ENSP00000325395.5:n.*1887G=
ENST00000350303.9:c.1866G= ENSP00000344152.5:p.Arg622=
ENST00000356839.9:c.1932G= ENSP00000349297.5:p.Arg644=
ENST00000542255.6:c.811G=
ENST00000543245.6:c.2001G= ENSP00000438689.2:p.Arg667=
ENST00000578033.1:n.357G=
ENST00000578319.5:n.513G=
ENST00000578711.1:n.1557G=
ENST00000578809.5:n.504G=
ENST00000579425.5:n.1048G=
ENST00000583848.5:c.298G= ENSP00000466487.1:n.298G=
ENST00000583850.5:n.703G=
ENST00000583858.5:c.863G=
NM_000018.3:c.1932G= NP_000009.1:p.Arg644=
NM_001033859.2:c.1866G= NP_001029031.1:p.Arg622=
NM_001270447.1:c.2001G= NP_001257376.1:p.Arg667=
NM_001270448.1:c.1704G= NP_001257377.1:p.Arg568=
XM_006721516.2:c.1953G= XP_006721579.2:p.Arg651=
XM_011523829.1:c.1851G= XP_011522131.1:p.Arg617=
XM_011523830.1:c.1830G= XP_011522132.1:p.Arg610=
XR_934021.1:n.2035G=
XR_934022.1:n.1941G=
XR_934023.1:n.1962G=
XM_006721516.3:c.1953G= XP_006721579.2:p.Arg651=
XM_011523829.2:c.1851G= XP_011522131.1:p.Arg617=
XM_011523830.2:c.1830G= XP_011522132.1:p.Arg610=
XM_024450741.1:c.1920G= XP_024306509.1:p.Arg640=
XR_934021.2:n.1987G=
XR_934022.2:n.1893G=
XR_934023.2:n.1914G=
NM_000018.4:c.1932G= MANE Select NP_000009.1:p.Arg644=
NM_001033859.3:c.1866G= NP_001029031.1:p.Arg622=
NM_001270447.2:c.2001G= NP_001257376.1:p.Arg667=
NM_001270448.2:c.1704G= NP_001257377.1:p.Arg568=