Canonical Allele Identifier: CA2245716383
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225039T= , CM000679.2:g.7225039T= GRCh38
NC_000017.10:g.7128358T= , CM000679.1:g.7128358T= GRCh37
NC_000017.9:g.7069082T= NCBI36
NG_007975.1:g.10206T=
NG_008391.2:g.12A=
NG_033038.1:g.14506A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1910T= MANE Select ENSP00000349297.5:p.Ile637=
ENST00000322910.9:c.*1865T= ENSP00000325395.5:n.*1865T=
ENST00000350303.9:c.1844T= ENSP00000344152.5:p.Ile615=
ENST00000356839.9:c.1910T= ENSP00000349297.5:p.Ile637=
ENST00000542255.6:c.789T=
ENST00000543245.6:c.1979T= ENSP00000438689.2:p.Ile660=
ENST00000578033.1:n.335T=
ENST00000578319.5:n.491T=
ENST00000578711.1:n.1535T=
ENST00000578809.5:n.482T=
ENST00000579425.5:n.1026T=
ENST00000583848.5:c.276T= ENSP00000466487.1:n.276T=
ENST00000583850.5:n.681T=
ENST00000583858.5:c.841T=
NM_000018.3:c.1910T= NP_000009.1:p.Ile637=
NM_001033859.2:c.1844T= NP_001029031.1:p.Ile615=
NM_001270447.1:c.1979T= NP_001257376.1:p.Ile660=
NM_001270448.1:c.1682T= NP_001257377.1:p.Ile561=
XM_006721516.2:c.1931T= XP_006721579.2:p.Ile644=
XM_011523829.1:c.1829T= XP_011522131.1:p.Ile610=
XM_011523830.1:c.1808T= XP_011522132.1:p.Ile603=
XR_934021.1:n.2013T=
XR_934022.1:n.1919T=
XR_934023.1:n.1940T=
XM_006721516.3:c.1931T= XP_006721579.2:p.Ile644=
XM_011523829.2:c.1829T= XP_011522131.1:p.Ile610=
XM_011523830.2:c.1808T= XP_011522132.1:p.Ile603=
XM_024450741.1:c.1898T= XP_024306509.1:p.Ile633=
XR_934021.2:n.1965T=
XR_934022.2:n.1871T=
XR_934023.2:n.1892T=
NM_000018.4:c.1910T= MANE Select NP_000009.1:p.Ile637=
NM_001033859.3:c.1844T= NP_001029031.1:p.Ile615=
NM_001270447.2:c.1979T= NP_001257376.1:p.Ile660=
NM_001270448.2:c.1682T= NP_001257377.1:p.Ile561=