Canonical Allele Identifier: CA2245716423
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225053G= , CM000679.2:g.7225053G= GRCh38
NC_000017.10:g.7128372G= , CM000679.1:g.7128372G= GRCh37
NC_000017.9:g.7069096G= NCBI36
NG_007975.1:g.10220G=
NG_033038.1:g.14492C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1924G= MANE Select ENSP00000349297.5:p.Val642=
ENST00000322910.9:c.*1879G= ENSP00000325395.5:n.*1879G=
ENST00000350303.9:c.1858G= ENSP00000344152.5:p.Val620=
ENST00000356839.9:c.1924G= ENSP00000349297.5:p.Val642=
ENST00000542255.6:c.803G=
ENST00000543245.6:c.1993G= ENSP00000438689.2:p.Val665=
ENST00000578033.1:n.349G=
ENST00000578319.5:n.505G=
ENST00000578711.1:n.1549G=
ENST00000578809.5:n.496G=
ENST00000579425.5:n.1040G=
ENST00000583848.5:c.290G= ENSP00000466487.1:n.290G=
ENST00000583850.5:n.695G=
ENST00000583858.5:c.855G=
NM_000018.3:c.1924G= NP_000009.1:p.Val642=
NM_001033859.2:c.1858G= NP_001029031.1:p.Val620=
NM_001270447.1:c.1993G= NP_001257376.1:p.Val665=
NM_001270448.1:c.1696G= NP_001257377.1:p.Val566=
XM_006721516.2:c.1945G= XP_006721579.2:p.Val649=
XM_011523829.1:c.1843G= XP_011522131.1:p.Val615=
XM_011523830.1:c.1822G= XP_011522132.1:p.Val608=
XR_934021.1:n.2027G=
XR_934022.1:n.1933G=
XR_934023.1:n.1954G=
XM_006721516.3:c.1945G= XP_006721579.2:p.Val649=
XM_011523829.2:c.1843G= XP_011522131.1:p.Val615=
XM_011523830.2:c.1822G= XP_011522132.1:p.Val608=
XM_024450741.1:c.1912G= XP_024306509.1:p.Val638=
XR_934021.2:n.1979G=
XR_934022.2:n.1885G=
XR_934023.2:n.1906G=
NM_000018.4:c.1924G= MANE Select NP_000009.1:p.Val642=
NM_001033859.3:c.1858G= NP_001029031.1:p.Val620=
NM_001270447.2:c.1993G= NP_001257376.1:p.Val665=
NM_001270448.2:c.1696G= NP_001257377.1:p.Val566=