Canonical Allele Identifier: CA2245700154
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221586A= , CM000679.2:g.7221586A= GRCh38
NC_000017.10:g.7124905A= , CM000679.1:g.7124905A= GRCh37
NC_000017.9:g.7065629A= NCBI36
NG_007975.1:g.6753A=
NG_008391.2:g.3465T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.526A= MANE Select ENSP00000349297.5:p.Ile176=
ENST00000322910.9:c.*481A= ENSP00000325395.5:n.*481A=
ENST00000350303.9:c.460A= ENSP00000344152.5:p.Ile154=
ENST00000356839.9:c.526A= ENSP00000349297.5:p.Ile176=
ENST00000543245.6:c.595A= ENSP00000438689.2:p.Ile199=
ENST00000577191.5:n.603A=
ENST00000577433.5:n.734A=
ENST00000577857.5:n.342A=
ENST00000579286.5:n.707A=
ENST00000579886.2:c.364A= ENSP00000463246.1:p.Ile122=
ENST00000580365.1:n.257A=
ENST00000581378.5:c.244A=
ENST00000581562.5:n.525-366A=
ENST00000582166.1:n.507A=
ENST00000583312.5:c.526A= ENSP00000467920.1:p.Ile176=
ENST00000583760.1:n.308A=
NM_000018.3:c.526A= NP_000009.1:p.Ile176=
NM_001033859.2:c.460A= NP_001029031.1:p.Ile154=
NM_001270447.1:c.595A= NP_001257376.1:p.Ile199=
NM_001270448.1:c.298A= NP_001257377.1:p.Ile100=
XM_006721516.2:c.526A= XP_006721579.2:p.Ile176=
XM_011523829.1:c.526A= XP_011522131.1:p.Ile176=
XM_011523830.1:c.526A= XP_011522132.1:p.Ile176=
XR_934021.1:n.633A=
XR_934022.1:n.633A=
XR_934023.1:n.633A=
XM_006721516.3:c.526A= XP_006721579.2:p.Ile176=
XM_011523829.2:c.526A= XP_011522131.1:p.Ile176=
XM_011523830.2:c.526A= XP_011522132.1:p.Ile176=
XM_024450741.1:c.526A= XP_024306509.1:p.Ile176=
XR_934021.2:n.585A=
XR_934022.2:n.585A=
XR_934023.2:n.585A=
NM_000018.4:c.526A= MANE Select NP_000009.1:p.Ile176=
NM_001033859.3:c.460A= NP_001029031.1:p.Ile154=
NM_001270447.2:c.595A= NP_001257376.1:p.Ile199=
NM_001270448.2:c.298A= NP_001257377.1:p.Ile100=