Canonical Allele Identifier: CA2245716472
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225066G= , CM000679.2:g.7225066G= GRCh38
NC_000017.10:g.7128385G= , CM000679.1:g.7128385G= GRCh37
NC_000017.9:g.7069109G= NCBI36
NG_007975.1:g.10233G=
NG_033038.1:g.14479C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1937G= MANE Select ENSP00000349297.5:p.Gly646=
ENST00000322910.9:c.*1892G= ENSP00000325395.5:n.*1892G=
ENST00000350303.9:c.1871G= ENSP00000344152.5:p.Gly624=
ENST00000356839.9:c.1937G= ENSP00000349297.5:p.Gly646=
ENST00000542255.6:c.816G=
ENST00000543245.6:c.2006G= ENSP00000438689.2:p.Gly669=
ENST00000578033.1:n.362G=
ENST00000578319.5:n.518G=
ENST00000578711.1:n.1562G=
ENST00000578809.5:n.509G=
ENST00000579425.5:n.1053G=
ENST00000583848.5:c.303G= ENSP00000466487.1:n.303G=
ENST00000583850.5:n.708G=
ENST00000583858.5:c.868G=
NM_000018.3:c.1937G= NP_000009.1:p.Gly646=
NM_001033859.2:c.1871G= NP_001029031.1:p.Gly624=
NM_001270447.1:c.2006G= NP_001257376.1:p.Gly669=
NM_001270448.1:c.1709G= NP_001257377.1:p.Gly570=
XM_006721516.2:c.1958G= XP_006721579.2:p.Gly653=
XM_011523829.1:c.1856G= XP_011522131.1:p.Gly619=
XM_011523830.1:c.1835G= XP_011522132.1:p.Gly612=
XR_934021.1:n.2040G=
XR_934022.1:n.1946G=
XR_934023.1:n.1967G=
XM_006721516.3:c.1958G= XP_006721579.2:p.Gly653=
XM_011523829.2:c.1856G= XP_011522131.1:p.Gly619=
XM_011523830.2:c.1835G= XP_011522132.1:p.Gly612=
XM_024450741.1:c.1925G= XP_024306509.1:p.Gly642=
XR_934021.2:n.1992G=
XR_934022.2:n.1898G=
XR_934023.2:n.1919G=
NM_000018.4:c.1937G= MANE Select NP_000009.1:p.Gly646=
NM_001033859.3:c.1871G= NP_001029031.1:p.Gly624=
NM_001270447.2:c.2006G= NP_001257376.1:p.Gly669=
NM_001270448.2:c.1709G= NP_001257377.1:p.Gly570=