Canonical Allele Identifier: CA2245716489
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225068G= , CM000679.2:g.7225068G= GRCh38
NC_000017.10:g.7128387G= , CM000679.1:g.7128387G= GRCh37
NC_000017.9:g.7069111G= NCBI36
NG_007975.1:g.10235G=
NG_033038.1:g.14477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1939G= MANE Select ENSP00000349297.5:p.Val647=
ENST00000322910.9:c.*1894G= ENSP00000325395.5:n.*1894G=
ENST00000350303.9:c.1873G= ENSP00000344152.5:p.Val625=
ENST00000356839.9:c.1939G= ENSP00000349297.5:p.Val647=
ENST00000542255.6:c.818G=
ENST00000543245.6:c.2008G= ENSP00000438689.2:p.Val670=
ENST00000578033.1:n.364G=
ENST00000578319.5:n.520G=
ENST00000578711.1:n.1564G=
ENST00000578809.5:n.511G=
ENST00000579425.5:n.1055G=
ENST00000583848.5:c.305G= ENSP00000466487.1:n.305G=
ENST00000583850.5:n.710G=
ENST00000583858.5:c.870G=
NM_000018.3:c.1939G= NP_000009.1:p.Val647=
NM_001033859.2:c.1873G= NP_001029031.1:p.Val625=
NM_001270447.1:c.2008G= NP_001257376.1:p.Val670=
NM_001270448.1:c.1711G= NP_001257377.1:p.Val571=
XM_006721516.2:c.1960G= XP_006721579.2:p.Val654=
XM_011523829.1:c.1858G= XP_011522131.1:p.Val620=
XM_011523830.1:c.1837G= XP_011522132.1:p.Val613=
XR_934021.1:n.2042G=
XR_934022.1:n.1948G=
XR_934023.1:n.1969G=
XM_006721516.3:c.1960G= XP_006721579.2:p.Val654=
XM_011523829.2:c.1858G= XP_011522131.1:p.Val620=
XM_011523830.2:c.1837G= XP_011522132.1:p.Val613=
XM_024450741.1:c.1927G= XP_024306509.1:p.Val643=
XR_934021.2:n.1994G=
XR_934022.2:n.1900G=
XR_934023.2:n.1921G=
NM_000018.4:c.1939G= MANE Select NP_000009.1:p.Val647=
NM_001033859.3:c.1873G= NP_001029031.1:p.Val625=
NM_001270447.2:c.2008G= NP_001257376.1:p.Val670=
NM_001270448.2:c.1711G= NP_001257377.1:p.Val571=