Canonical Allele Identifier: CA2245700954
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222033G= , CM000679.2:g.7222033G= GRCh38
NC_000017.10:g.7125352G= , CM000679.1:g.7125352G= GRCh37
NC_000017.9:g.7066076G= NCBI36
NG_007975.1:g.7200G=
NG_008391.2:g.3018C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.704G= MANE Select ENSP00000349297.5:p.Ser235=
ENST00000322910.9:c.*659G= ENSP00000325395.5:n.*659G=
ENST00000350303.9:c.638G= ENSP00000344152.5:p.Ser213=
ENST00000356839.9:c.704G= ENSP00000349297.5:p.Ser235=
ENST00000543245.6:c.773G= ENSP00000438689.2:p.Ser258=
ENST00000577191.5:n.781G=
ENST00000577857.5:n.520G=
ENST00000579286.5:n.885G=
ENST00000580365.1:n.435G=
ENST00000581378.5:c.422G=
ENST00000582379.1:n.88G=
ENST00000583760.1:n.486G=
NM_000018.3:c.704G= NP_000009.1:p.Ser235=
NM_001033859.2:c.638G= NP_001029031.1:p.Ser213=
NM_001270447.1:c.773G= NP_001257376.1:p.Ser258=
NM_001270448.1:c.476G= NP_001257377.1:p.Ser159=
XM_006721516.2:c.704G= XP_006721579.2:p.Ser235=
XM_011523829.1:c.704G= XP_011522131.1:p.Ser235=
XM_011523830.1:c.704G= XP_011522132.1:p.Ser235=
XR_934021.1:n.811G=
XR_934022.1:n.811G=
XR_934023.1:n.811G=
XM_006721516.3:c.704G= XP_006721579.2:p.Ser235=
XM_011523829.2:c.704G= XP_011522131.1:p.Ser235=
XM_011523830.2:c.704G= XP_011522132.1:p.Ser235=
XM_024450741.1:c.704G= XP_024306509.1:p.Ser235=
XR_934021.2:n.763G=
XR_934022.2:n.763G=
XR_934023.2:n.763G=
NM_000018.4:c.704G= MANE Select NP_000009.1:p.Ser235=
NM_001033859.3:c.638G= NP_001029031.1:p.Ser213=
NM_001270447.2:c.773G= NP_001257376.1:p.Ser258=
NM_001270448.2:c.476G= NP_001257377.1:p.Ser159=