Canonical Allele Identifier: CA2245700367
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221647C= , CM000679.2:g.7221647C= GRCh38
NC_000017.10:g.7124966C= , CM000679.1:g.7124966C= GRCh37
NC_000017.9:g.7065690C= NCBI36
NG_007975.1:g.6814C=
NG_008391.2:g.3404G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.587C= MANE Select ENSP00000349297.5:p.Ala196=
ENST00000322910.9:c.*542C= ENSP00000325395.5:n.*542C=
ENST00000350303.9:c.521C= ENSP00000344152.5:p.Ala174=
ENST00000356839.9:c.587C= ENSP00000349297.5:p.Ala196=
ENST00000543245.6:c.656C= ENSP00000438689.2:p.Ala219=
ENST00000577191.5:n.664C=
ENST00000577433.5:n.795C=
ENST00000577857.5:n.403C=
ENST00000579286.5:n.768C=
ENST00000579886.2:c.425C= ENSP00000463246.1:p.Ala142=
ENST00000580365.1:n.318C=
ENST00000581378.5:c.305C=
ENST00000581562.5:n.525-305C=
ENST00000583312.5:c.587C= ENSP00000467920.1:p.Ala196=
ENST00000583760.1:n.369C=
NM_000018.3:c.587C= NP_000009.1:p.Ala196=
NM_001033859.2:c.521C= NP_001029031.1:p.Ala174=
NM_001270447.1:c.656C= NP_001257376.1:p.Ala219=
NM_001270448.1:c.359C= NP_001257377.1:p.Ala120=
XM_006721516.2:c.587C= XP_006721579.2:p.Ala196=
XM_011523829.1:c.587C= XP_011522131.1:p.Ala196=
XM_011523830.1:c.587C= XP_011522132.1:p.Ala196=
XR_934021.1:n.694C=
XR_934022.1:n.694C=
XR_934023.1:n.694C=
XM_006721516.3:c.587C= XP_006721579.2:p.Ala196=
XM_011523829.2:c.587C= XP_011522131.1:p.Ala196=
XM_011523830.2:c.587C= XP_011522132.1:p.Ala196=
XM_024450741.1:c.587C= XP_024306509.1:p.Ala196=
XR_934021.2:n.646C=
XR_934022.2:n.646C=
XR_934023.2:n.646C=
NM_000018.4:c.587C= MANE Select NP_000009.1:p.Ala196=
NM_001033859.3:c.521C= NP_001029031.1:p.Ala174=
NM_001270447.2:c.656C= NP_001257376.1:p.Ala219=
NM_001270448.2:c.359C= NP_001257377.1:p.Ala120=