Canonical Allele Identifier: CA2245700951
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222028G= , CM000679.2:g.7222028G= GRCh38
NC_000017.10:g.7125347G= , CM000679.1:g.7125347G= GRCh37
NC_000017.9:g.7066071G= NCBI36
NG_007975.1:g.7195G=
NG_008391.2:g.3023C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.699G= MANE Select ENSP00000349297.5:p.Val233=
ENST00000322910.9:c.*654G= ENSP00000325395.5:n.*654G=
ENST00000350303.9:c.633G= ENSP00000344152.5:p.Val211=
ENST00000356839.9:c.699G= ENSP00000349297.5:p.Val233=
ENST00000543245.6:c.768G= ENSP00000438689.2:p.Val256=
ENST00000577191.5:n.776G=
ENST00000577857.5:n.515G=
ENST00000579286.5:n.880G=
ENST00000580365.1:n.430G=
ENST00000581378.5:c.417G=
ENST00000582379.1:n.83G=
ENST00000583760.1:n.481G=
NM_000018.3:c.699G= NP_000009.1:p.Val233=
NM_001033859.2:c.633G= NP_001029031.1:p.Val211=
NM_001270447.1:c.768G= NP_001257376.1:p.Val256=
NM_001270448.1:c.471G= NP_001257377.1:p.Val157=
XM_006721516.2:c.699G= XP_006721579.2:p.Val233=
XM_011523829.1:c.699G= XP_011522131.1:p.Val233=
XM_011523830.1:c.699G= XP_011522132.1:p.Val233=
XR_934021.1:n.806G=
XR_934022.1:n.806G=
XR_934023.1:n.806G=
XM_006721516.3:c.699G= XP_006721579.2:p.Val233=
XM_011523829.2:c.699G= XP_011522131.1:p.Val233=
XM_011523830.2:c.699G= XP_011522132.1:p.Val233=
XM_024450741.1:c.699G= XP_024306509.1:p.Val233=
XR_934021.2:n.758G=
XR_934022.2:n.758G=
XR_934023.2:n.758G=
NM_000018.4:c.699G= MANE Select NP_000009.1:p.Val233=
NM_001033859.3:c.633G= NP_001029031.1:p.Val211=
NM_001270447.2:c.768G= NP_001257376.1:p.Val256=
NM_001270448.2:c.471G= NP_001257377.1:p.Val157=