Canonical Allele Identifier: CA2245716564
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225090G= , CM000679.2:g.7225090G= GRCh38
NC_000017.10:g.7128409G= , CM000679.1:g.7128409G= GRCh37
NC_000017.9:g.7069133G= NCBI36
NG_007975.1:g.10257G=
NG_033038.1:g.14455C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1961G= MANE Select ENSP00000349297.5:p.Gly654=
ENST00000322910.9:c.*1916G= ENSP00000325395.5:n.*1916G=
ENST00000350303.9:c.1895G= ENSP00000344152.5:p.Gly632=
ENST00000356839.9:c.1961G= ENSP00000349297.5:p.Gly654=
ENST00000542255.6:c.840G=
ENST00000543245.6:c.2030G= ENSP00000438689.2:p.Gly677=
ENST00000578033.1:n.386G=
ENST00000578319.5:n.542G=
ENST00000578711.1:n.1586G=
ENST00000578809.5:n.533G=
ENST00000579425.5:n.1077G=
ENST00000583848.5:c.327G= ENSP00000466487.1:n.327G=
ENST00000583850.5:n.732G=
ENST00000583858.5:c.892G=
NM_000018.3:c.1961G= NP_000009.1:p.Gly654=
NM_001033859.2:c.1895G= NP_001029031.1:p.Gly632=
NM_001270447.1:c.2030G= NP_001257376.1:p.Gly677=
NM_001270448.1:c.1733G= NP_001257377.1:p.Gly578=
XM_006721516.2:c.1982G= XP_006721579.2:p.Gly661=
XM_011523829.1:c.1880G= XP_011522131.1:p.Gly627=
XM_011523830.1:c.1859G= XP_011522132.1:p.Gly620=
XR_934021.1:n.2064G=
XR_934022.1:n.1970G=
XR_934023.1:n.1991G=
XM_006721516.3:c.1982G= XP_006721579.2:p.Gly661=
XM_011523829.2:c.1880G= XP_011522131.1:p.Gly627=
XM_011523830.2:c.1859G= XP_011522132.1:p.Gly620=
XM_024450741.1:c.1949G= XP_024306509.1:p.Gly650=
XR_934021.2:n.2016G=
XR_934022.2:n.1922G=
XR_934023.2:n.1943G=
NM_000018.4:c.1961G= MANE Select NP_000009.1:p.Gly654=
NM_001033859.3:c.1895G= NP_001029031.1:p.Gly632=
NM_001270447.2:c.2030G= NP_001257376.1:p.Gly677=
NM_001270448.2:c.1733G= NP_001257377.1:p.Gly578=