Canonical Allele Identifier: CA2245700829
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221978A= , CM000679.2:g.7221978A= GRCh38
NC_000017.10:g.7125297A= , CM000679.1:g.7125297A= GRCh37
NC_000017.9:g.7066021A= NCBI36
NG_007975.1:g.7145A=
NG_008391.2:g.3073T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.649A= MANE Select ENSP00000349297.5:p.Thr217=
ENST00000322910.9:c.*604A= ENSP00000325395.5:n.*604A=
ENST00000350303.9:c.583A= ENSP00000344152.5:p.Thr195=
ENST00000356839.9:c.649A= ENSP00000349297.5:p.Thr217=
ENST00000543245.6:c.718A= ENSP00000438689.2:p.Thr240=
ENST00000577191.5:n.726A=
ENST00000577857.5:n.465A=
ENST00000579286.5:n.830A=
ENST00000580365.1:n.380A=
ENST00000581378.5:c.367A=
ENST00000581562.5:n.551A=
ENST00000582379.1:n.33A=
ENST00000583312.5:c.664A= ENSP00000467920.1:p.Thr222=
ENST00000583760.1:n.431A=
NM_000018.3:c.649A= NP_000009.1:p.Thr217=
NM_001033859.2:c.583A= NP_001029031.1:p.Thr195=
NM_001270447.1:c.718A= NP_001257376.1:p.Thr240=
NM_001270448.1:c.421A= NP_001257377.1:p.Thr141=
XM_006721516.2:c.649A= XP_006721579.2:p.Thr217=
XM_011523829.1:c.649A= XP_011522131.1:p.Thr217=
XM_011523830.1:c.649A= XP_011522132.1:p.Thr217=
XR_934021.1:n.756A=
XR_934022.1:n.756A=
XR_934023.1:n.756A=
XM_006721516.3:c.649A= XP_006721579.2:p.Thr217=
XM_011523829.2:c.649A= XP_011522131.1:p.Thr217=
XM_011523830.2:c.649A= XP_011522132.1:p.Thr217=
XM_024450741.1:c.649A= XP_024306509.1:p.Thr217=
XR_934021.2:n.708A=
XR_934022.2:n.708A=
XR_934023.2:n.708A=
NM_000018.4:c.649A= MANE Select NP_000009.1:p.Thr217=
NM_001033859.3:c.583A= NP_001029031.1:p.Thr195=
NM_001270447.2:c.718A= NP_001257376.1:p.Thr240=
NM_001270448.2:c.421A= NP_001257377.1:p.Thr141=