Canonical Allele Identifier: CA2245700956
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222034C= , CM000679.2:g.7222034C= GRCh38
NC_000017.10:g.7125353C= , CM000679.1:g.7125353C= GRCh37
NC_000017.9:g.7066077C= NCBI36
NG_007975.1:g.7201C=
NG_008391.2:g.3017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.705C= MANE Select ENSP00000349297.5:p.Ser235=
ENST00000322910.9:c.*660C= ENSP00000325395.5:n.*660C=
ENST00000350303.9:c.639C= ENSP00000344152.5:p.Ser213=
ENST00000356839.9:c.705C= ENSP00000349297.5:p.Ser235=
ENST00000543245.6:c.774C= ENSP00000438689.2:p.Ser258=
ENST00000577191.5:n.782C=
ENST00000577857.5:n.521C=
ENST00000579286.5:n.886C=
ENST00000580365.1:n.436C=
ENST00000581378.5:c.423C=
ENST00000582379.1:n.89C=
ENST00000583760.1:n.487C=
NM_000018.3:c.705C= NP_000009.1:p.Ser235=
NM_001033859.2:c.639C= NP_001029031.1:p.Ser213=
NM_001270447.1:c.774C= NP_001257376.1:p.Ser258=
NM_001270448.1:c.477C= NP_001257377.1:p.Ser159=
XM_006721516.2:c.705C= XP_006721579.2:p.Ser235=
XM_011523829.1:c.705C= XP_011522131.1:p.Ser235=
XM_011523830.1:c.705C= XP_011522132.1:p.Ser235=
XR_934021.1:n.812C=
XR_934022.1:n.812C=
XR_934023.1:n.812C=
XM_006721516.3:c.705C= XP_006721579.2:p.Ser235=
XM_011523829.2:c.705C= XP_011522131.1:p.Ser235=
XM_011523830.2:c.705C= XP_011522132.1:p.Ser235=
XM_024450741.1:c.705C= XP_024306509.1:p.Ser235=
XR_934021.2:n.764C=
XR_934022.2:n.764C=
XR_934023.2:n.764C=
NM_000018.4:c.705C= MANE Select NP_000009.1:p.Ser235=
NM_001033859.3:c.639C= NP_001029031.1:p.Ser213=
NM_001270447.2:c.774C= NP_001257376.1:p.Ser258=
NM_001270448.2:c.477C= NP_001257377.1:p.Ser159=