Canonical Allele Identifier: CA2245697705
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220171C= , CM000679.2:g.7220171C= GRCh38
NC_000017.10:g.7123490C= , CM000679.1:g.7123490C= GRCh37
NC_000017.9:g.7064214C= NCBI36
NG_007975.1:g.5338C=
NG_008391.2:g.4880G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.112C= MANE Select ENSP00000349297.5:p.Arg38=
ENST00000322910.9:c.*67C= ENSP00000325395.5:n.*67C=
ENST00000350303.9:c.112C= ENSP00000344152.5:p.Arg38=
ENST00000356839.9:c.112C= ENSP00000349297.5:p.Arg38=
ENST00000543245.6:c.181C= ENSP00000438689.2:p.Arg61=
ENST00000577191.5:n.189C=
ENST00000577857.5:n.202C=
ENST00000578269.5:n.219C=
ENST00000578421.1:n.246C=
ENST00000579286.5:n.219C=
ENST00000579886.2:c.112C= ENSP00000463246.1:p.Arg38=
ENST00000580263.5:n.202C=
ENST00000581562.5:n.159C=
ENST00000582056.5:n.202C=
ENST00000582356.5:n.237C=
ENST00000583312.5:c.112C= ENSP00000467920.1:p.Arg38=
ENST00000584103.5:c.112C= ENSP00000465353.1:p.Arg38=
NM_000018.3:c.112C= NP_000009.1:p.Arg38=
NM_001033859.2:c.112C= NP_001029031.1:p.Arg38=
NM_001270447.1:c.181C= NP_001257376.1:p.Arg61=
NM_001270448.1:c.-117C= NP_001257377.1:n.-117C=
XM_006721516.2:c.112C= XP_006721579.2:p.Arg38=
XM_011523829.1:c.112C= XP_011522131.1:p.Arg38=
XM_011523830.1:c.112C= XP_011522132.1:p.Arg38=
XR_934021.1:n.219C=
XR_934022.1:n.219C=
XR_934023.1:n.219C=
XM_006721516.3:c.112C= XP_006721579.2:p.Arg38=
XM_011523829.2:c.112C= XP_011522131.1:p.Arg38=
XM_011523830.2:c.112C= XP_011522132.1:p.Arg38=
XM_024450741.1:c.112C= XP_024306509.1:p.Arg38=
XR_934021.2:n.171C=
XR_934022.2:n.171C=
XR_934023.2:n.171C=
NM_000018.4:c.112C= MANE Select NP_000009.1:p.Arg38=
NM_001033859.3:c.112C= NP_001029031.1:p.Arg38=
NM_001270447.2:c.181C= NP_001257376.1:p.Arg61=
NM_001270448.2:c.-117C= NP_001257377.1:n.-117C=