Canonical Allele Identifier: CA2245700348
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221642A= , CM000679.2:g.7221642A= GRCh38
NC_000017.10:g.7124961A= , CM000679.1:g.7124961A= GRCh37
NC_000017.9:g.7065685A= NCBI36
NG_007975.1:g.6809A=
NG_008391.2:g.3409T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.582A= MANE Select ENSP00000349297.5:p.Thr194=
ENST00000322910.9:c.*537A= ENSP00000325395.5:n.*537A=
ENST00000350303.9:c.516A= ENSP00000344152.5:p.Thr172=
ENST00000356839.9:c.582A= ENSP00000349297.5:p.Thr194=
ENST00000543245.6:c.651A= ENSP00000438689.2:p.Thr217=
ENST00000577191.5:n.659A=
ENST00000577433.5:n.790A=
ENST00000577857.5:n.398A=
ENST00000579286.5:n.763A=
ENST00000579886.2:c.420A= ENSP00000463246.1:p.Thr140=
ENST00000580365.1:n.313A=
ENST00000581378.5:c.300A=
ENST00000581562.5:n.525-310A=
ENST00000583312.5:c.582A= ENSP00000467920.1:p.Thr194=
ENST00000583760.1:n.364A=
NM_000018.3:c.582A= NP_000009.1:p.Thr194=
NM_001033859.2:c.516A= NP_001029031.1:p.Thr172=
NM_001270447.1:c.651A= NP_001257376.1:p.Thr217=
NM_001270448.1:c.354A= NP_001257377.1:p.Thr118=
XM_006721516.2:c.582A= XP_006721579.2:p.Thr194=
XM_011523829.1:c.582A= XP_011522131.1:p.Thr194=
XM_011523830.1:c.582A= XP_011522132.1:p.Thr194=
XR_934021.1:n.689A=
XR_934022.1:n.689A=
XR_934023.1:n.689A=
XM_006721516.3:c.582A= XP_006721579.2:p.Thr194=
XM_011523829.2:c.582A= XP_011522131.1:p.Thr194=
XM_011523830.2:c.582A= XP_011522132.1:p.Thr194=
XM_024450741.1:c.582A= XP_024306509.1:p.Thr194=
XR_934021.2:n.641A=
XR_934022.2:n.641A=
XR_934023.2:n.641A=
NM_000018.4:c.582A= MANE Select NP_000009.1:p.Thr194=
NM_001033859.3:c.516A= NP_001029031.1:p.Thr172=
NM_001270447.2:c.651A= NP_001257376.1:p.Thr217=
NM_001270448.2:c.354A= NP_001257377.1:p.Thr118=