Canonical Allele Identifier: CA2245699248
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221001G= , CM000679.2:g.7221001G= GRCh38
NC_000017.10:g.7124320G= , CM000679.1:g.7124320G= GRCh37
NC_000017.9:g.7065044G= NCBI36
NG_007975.1:g.6168G=
NG_008391.2:g.4050C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.420G= MANE Select ENSP00000349297.5:p.Gly140=
ENST00000322910.9:c.*375G= ENSP00000325395.5:n.*375G=
ENST00000350303.9:c.354G= ENSP00000344152.5:p.Gly118=
ENST00000356839.9:c.420G= ENSP00000349297.5:p.Gly140=
ENST00000543245.6:c.489G= ENSP00000438689.2:p.Gly163=
ENST00000577191.5:n.497G=
ENST00000577433.5:n.628G=
ENST00000577857.5:n.293+171G=
ENST00000579286.5:n.601G=
ENST00000579886.2:c.258G= ENSP00000463246.1:p.Gly86=
ENST00000580365.1:n.151G=
ENST00000581378.5:c.119G=
ENST00000581562.5:n.467G=
ENST00000582056.5:n.603G=
ENST00000582166.1:n.401G=
ENST00000583312.5:c.420G= ENSP00000467920.1:p.Gly140=
ENST00000584103.5:c.453G= ENSP00000465353.1:p.Gly151=
NM_000018.3:c.420G= NP_000009.1:p.Gly140=
NM_001033859.2:c.354G= NP_001029031.1:p.Gly118=
NM_001270447.1:c.489G= NP_001257376.1:p.Gly163=
NM_001270448.1:c.192G= NP_001257377.1:p.Gly64=
XM_006721516.2:c.420G= XP_006721579.2:p.Gly140=
XM_011523829.1:c.420G= XP_011522131.1:p.Gly140=
XM_011523830.1:c.420G= XP_011522132.1:p.Gly140=
XR_934021.1:n.527G=
XR_934022.1:n.527G=
XR_934023.1:n.527G=
XM_006721516.3:c.420G= XP_006721579.2:p.Gly140=
XM_011523829.2:c.420G= XP_011522131.1:p.Gly140=
XM_011523830.2:c.420G= XP_011522132.1:p.Gly140=
XM_024450741.1:c.420G= XP_024306509.1:p.Gly140=
XR_934021.2:n.479G=
XR_934022.2:n.479G=
XR_934023.2:n.479G=
NM_000018.4:c.420G= MANE Select NP_000009.1:p.Gly140=
NM_001033859.3:c.354G= NP_001029031.1:p.Gly118=
NM_001270447.2:c.489G= NP_001257376.1:p.Gly163=
NM_001270448.2:c.192G= NP_001257377.1:p.Gly64=