Canonical Allele Identifier: CA2245716441
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225059C= , CM000679.2:g.7225059C= GRCh38
NC_000017.10:g.7128378C= , CM000679.1:g.7128378C= GRCh37
NC_000017.9:g.7069102C= NCBI36
NG_007975.1:g.10226C=
NG_033038.1:g.14486G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1930C= MANE Select ENSP00000349297.5:p.Arg644=
ENST00000322910.9:c.*1885C= ENSP00000325395.5:n.*1885C=
ENST00000350303.9:c.1864C= ENSP00000344152.5:p.Arg622=
ENST00000356839.9:c.1930C= ENSP00000349297.5:p.Arg644=
ENST00000542255.6:c.809C=
ENST00000543245.6:c.1999C= ENSP00000438689.2:p.Arg667=
ENST00000578033.1:n.355C=
ENST00000578319.5:n.511C=
ENST00000578711.1:n.1555C=
ENST00000578809.5:n.502C=
ENST00000579425.5:n.1046C=
ENST00000583848.5:c.296C= ENSP00000466487.1:n.296C=
ENST00000583850.5:n.701C=
ENST00000583858.5:c.861C=
NM_000018.3:c.1930C= NP_000009.1:p.Arg644=
NM_001033859.2:c.1864C= NP_001029031.1:p.Arg622=
NM_001270447.1:c.1999C= NP_001257376.1:p.Arg667=
NM_001270448.1:c.1702C= NP_001257377.1:p.Arg568=
XM_006721516.2:c.1951C= XP_006721579.2:p.Arg651=
XM_011523829.1:c.1849C= XP_011522131.1:p.Arg617=
XM_011523830.1:c.1828C= XP_011522132.1:p.Arg610=
XR_934021.1:n.2033C=
XR_934022.1:n.1939C=
XR_934023.1:n.1960C=
XM_006721516.3:c.1951C= XP_006721579.2:p.Arg651=
XM_011523829.2:c.1849C= XP_011522131.1:p.Arg617=
XM_011523830.2:c.1828C= XP_011522132.1:p.Arg610=
XM_024450741.1:c.1918C= XP_024306509.1:p.Arg640=
XR_934021.2:n.1985C=
XR_934022.2:n.1891C=
XR_934023.2:n.1912C=
NM_000018.4:c.1930C= MANE Select NP_000009.1:p.Arg644=
NM_001033859.3:c.1864C= NP_001029031.1:p.Arg622=
NM_001270447.2:c.1999C= NP_001257376.1:p.Arg667=
NM_001270448.2:c.1702C= NP_001257377.1:p.Arg568=