Canonical Allele Identifier: CA2245699272
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221009G= , CM000679.2:g.7221009G= GRCh38
NC_000017.10:g.7124328G= , CM000679.1:g.7124328G= GRCh37
NC_000017.9:g.7065052G= NCBI36
NG_007975.1:g.6176G=
NG_008391.2:g.4042C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.428G= MANE Select ENSP00000349297.5:p.Gly143=
ENST00000322910.9:c.*383G= ENSP00000325395.5:n.*383G=
ENST00000350303.9:c.362G= ENSP00000344152.5:p.Gly121=
ENST00000356839.9:c.428G= ENSP00000349297.5:p.Gly143=
ENST00000543245.6:c.497G= ENSP00000438689.2:p.Gly166=
ENST00000577191.5:n.505G=
ENST00000577433.5:n.636G=
ENST00000577857.5:n.293+179G=
ENST00000579286.5:n.609G=
ENST00000579886.2:c.266G= ENSP00000463246.1:p.Gly89=
ENST00000580365.1:n.159G=
ENST00000581378.5:c.127G=
ENST00000581562.5:n.475G=
ENST00000582056.5:n.611G=
ENST00000582166.1:n.409G=
ENST00000583312.5:c.428G= ENSP00000467920.1:p.Gly143=
ENST00000584103.5:c.461G= ENSP00000465353.1:p.Gly154=
NM_000018.3:c.428G= NP_000009.1:p.Gly143=
NM_001033859.2:c.362G= NP_001029031.1:p.Gly121=
NM_001270447.1:c.497G= NP_001257376.1:p.Gly166=
NM_001270448.1:c.200G= NP_001257377.1:p.Gly67=
XM_006721516.2:c.428G= XP_006721579.2:p.Gly143=
XM_011523829.1:c.428G= XP_011522131.1:p.Gly143=
XM_011523830.1:c.428G= XP_011522132.1:p.Gly143=
XR_934021.1:n.535G=
XR_934022.1:n.535G=
XR_934023.1:n.535G=
XM_006721516.3:c.428G= XP_006721579.2:p.Gly143=
XM_011523829.2:c.428G= XP_011522131.1:p.Gly143=
XM_011523830.2:c.428G= XP_011522132.1:p.Gly143=
XM_024450741.1:c.428G= XP_024306509.1:p.Gly143=
XR_934021.2:n.487G=
XR_934022.2:n.487G=
XR_934023.2:n.487G=
NM_000018.4:c.428G= MANE Select NP_000009.1:p.Gly143=
NM_001033859.3:c.362G= NP_001029031.1:p.Gly121=
NM_001270447.2:c.497G= NP_001257376.1:p.Gly166=
NM_001270448.2:c.200G= NP_001257377.1:p.Gly67=