Canonical Allele Identifier: CA2245716479
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225067T= , CM000679.2:g.7225067T= GRCh38
NC_000017.10:g.7128386T= , CM000679.1:g.7128386T= GRCh37
NC_000017.9:g.7069110T= NCBI36
NG_007975.1:g.10234T=
NG_033038.1:g.14478A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1938T= MANE Select ENSP00000349297.5:p.Gly646=
ENST00000322910.9:c.*1893T= ENSP00000325395.5:n.*1893T=
ENST00000350303.9:c.1872T= ENSP00000344152.5:p.Gly624=
ENST00000356839.9:c.1938T= ENSP00000349297.5:p.Gly646=
ENST00000542255.6:c.817T=
ENST00000543245.6:c.2007T= ENSP00000438689.2:p.Gly669=
ENST00000578033.1:n.363T=
ENST00000578319.5:n.519T=
ENST00000578711.1:n.1563T=
ENST00000578809.5:n.510T=
ENST00000579425.5:n.1054T=
ENST00000583848.5:c.304T= ENSP00000466487.1:n.304T=
ENST00000583850.5:n.709T=
ENST00000583858.5:c.869T=
NM_000018.3:c.1938T= NP_000009.1:p.Gly646=
NM_001033859.2:c.1872T= NP_001029031.1:p.Gly624=
NM_001270447.1:c.2007T= NP_001257376.1:p.Gly669=
NM_001270448.1:c.1710T= NP_001257377.1:p.Gly570=
XM_006721516.2:c.1959T= XP_006721579.2:p.Gly653=
XM_011523829.1:c.1857T= XP_011522131.1:p.Gly619=
XM_011523830.1:c.1836T= XP_011522132.1:p.Gly612=
XR_934021.1:n.2041T=
XR_934022.1:n.1947T=
XR_934023.1:n.1968T=
XM_006721516.3:c.1959T= XP_006721579.2:p.Gly653=
XM_011523829.2:c.1857T= XP_011522131.1:p.Gly619=
XM_011523830.2:c.1836T= XP_011522132.1:p.Gly612=
XM_024450741.1:c.1926T= XP_024306509.1:p.Gly642=
XR_934021.2:n.1993T=
XR_934022.2:n.1899T=
XR_934023.2:n.1920T=
NM_000018.4:c.1938T= MANE Select NP_000009.1:p.Gly646=
NM_001033859.3:c.1872T= NP_001029031.1:p.Gly624=
NM_001270447.2:c.2007T= NP_001257376.1:p.Gly669=
NM_001270448.2:c.1710T= NP_001257377.1:p.Gly570=