Canonical Allele Identifier: CA2245709804
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222828C= , CM000679.2:g.7222828C= GRCh38
NC_000017.10:g.7126147C= , CM000679.1:g.7126147C= GRCh37
NC_000017.9:g.7066871C= NCBI36
NG_007975.1:g.7995C=
NG_008391.2:g.2223G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1040C= MANE Select ENSP00000349297.5:p.Ala347=
ENST00000322910.9:c.*995C= ENSP00000325395.5:n.*995C=
ENST00000350303.9:c.974C= ENSP00000344152.5:p.Ala325=
ENST00000356839.9:c.1040C= ENSP00000349297.5:p.Ala347=
ENST00000543245.6:c.1109C= ENSP00000438689.2:p.Ala370=
ENST00000578824.5:n.189C=
ENST00000582379.1:n.424C=
ENST00000583858.5:c.69C=
NM_000018.3:c.1040C= NP_000009.1:p.Ala347=
NM_001033859.2:c.974C= NP_001029031.1:p.Ala325=
NM_001270447.1:c.1109C= NP_001257376.1:p.Ala370=
NM_001270448.1:c.812C= NP_001257377.1:p.Ala271=
XM_006721516.2:c.1040C= XP_006721579.2:p.Ala347=
XM_011523829.1:c.1040C= XP_011522131.1:p.Ala347=
XM_011523830.1:c.1040C= XP_011522132.1:p.Ala347=
XR_934021.1:n.1147C=
XR_934022.1:n.1147C=
XR_934023.1:n.1147C=
XM_006721516.3:c.1040C= XP_006721579.2:p.Ala347=
XM_011523829.2:c.1040C= XP_011522131.1:p.Ala347=
XM_011523830.2:c.1040C= XP_011522132.1:p.Ala347=
XM_024450741.1:c.1040C= XP_024306509.1:p.Ala347=
XR_934021.2:n.1099C=
XR_934022.2:n.1099C=
XR_934023.2:n.1099C=
NM_000018.4:c.1040C= MANE Select NP_000009.1:p.Ala347=
NM_001033859.3:c.974C= NP_001029031.1:p.Ala325=
NM_001270447.2:c.1109C= NP_001257376.1:p.Ala370=
NM_001270448.2:c.812C= NP_001257377.1:p.Ala271=