Canonical Allele Identifier: CA2245699208
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220976C= , CM000679.2:g.7220976C= GRCh38
NC_000017.10:g.7124295C= , CM000679.1:g.7124295C= GRCh37
NC_000017.9:g.7065019C= NCBI36
NG_007975.1:g.6143C=
NG_008391.2:g.4075G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.395C= MANE Select ENSP00000349297.5:p.Thr132=
ENST00000322910.9:c.*350C= ENSP00000325395.5:n.*350C=
ENST00000350303.9:c.329C= ENSP00000344152.5:p.Thr110=
ENST00000356839.9:c.395C= ENSP00000349297.5:p.Thr132=
ENST00000543245.6:c.464C= ENSP00000438689.2:p.Thr155=
ENST00000577191.5:n.472C=
ENST00000577433.5:n.603C=
ENST00000577857.5:n.293+146C=
ENST00000579286.5:n.576C=
ENST00000579886.2:c.233C= ENSP00000463246.1:p.Thr78=
ENST00000580365.1:n.126C=
ENST00000581378.5:c.94C=
ENST00000581562.5:n.442C=
ENST00000582056.5:n.578C=
ENST00000582166.1:n.376C=
ENST00000583312.5:c.395C= ENSP00000467920.1:p.Thr132=
ENST00000584103.5:c.428C= ENSP00000465353.1:p.Thr143=
NM_000018.3:c.395C= NP_000009.1:p.Thr132=
NM_001033859.2:c.329C= NP_001029031.1:p.Thr110=
NM_001270447.1:c.464C= NP_001257376.1:p.Thr155=
NM_001270448.1:c.167C= NP_001257377.1:p.Thr56=
XM_006721516.2:c.395C= XP_006721579.2:p.Thr132=
XM_011523829.1:c.395C= XP_011522131.1:p.Thr132=
XM_011523830.1:c.395C= XP_011522132.1:p.Thr132=
XR_934021.1:n.502C=
XR_934022.1:n.502C=
XR_934023.1:n.502C=
XM_006721516.3:c.395C= XP_006721579.2:p.Thr132=
XM_011523829.2:c.395C= XP_011522131.1:p.Thr132=
XM_011523830.2:c.395C= XP_011522132.1:p.Thr132=
XM_024450741.1:c.395C= XP_024306509.1:p.Thr132=
XR_934021.2:n.454C=
XR_934022.2:n.454C=
XR_934023.2:n.454C=
NM_000018.4:c.395C= MANE Select NP_000009.1:p.Thr132=
NM_001033859.3:c.329C= NP_001029031.1:p.Thr110=
NM_001270447.2:c.464C= NP_001257376.1:p.Thr155=
NM_001270448.2:c.167C= NP_001257377.1:p.Thr56=