Canonical Allele Identifier: CA2245716525
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225082C= , CM000679.2:g.7225082C= GRCh38
NC_000017.10:g.7128401C= , CM000679.1:g.7128401C= GRCh37
NC_000017.9:g.7069125C= NCBI36
NG_007975.1:g.10249C=
NG_033038.1:g.14463G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1953C= MANE Select ENSP00000349297.5:p.Asn651=
ENST00000322910.9:c.*1908C= ENSP00000325395.5:n.*1908C=
ENST00000350303.9:c.1887C= ENSP00000344152.5:p.Asn629=
ENST00000356839.9:c.1953C= ENSP00000349297.5:p.Asn651=
ENST00000542255.6:c.832C=
ENST00000543245.6:c.2022C= ENSP00000438689.2:p.Asn674=
ENST00000578033.1:n.378C=
ENST00000578319.5:n.534C=
ENST00000578711.1:n.1578C=
ENST00000578809.5:n.525C=
ENST00000579425.5:n.1069C=
ENST00000583848.5:c.319C= ENSP00000466487.1:n.319C=
ENST00000583850.5:n.724C=
ENST00000583858.5:c.884C=
NM_000018.3:c.1953C= NP_000009.1:p.Asn651=
NM_001033859.2:c.1887C= NP_001029031.1:p.Asn629=
NM_001270447.1:c.2022C= NP_001257376.1:p.Asn674=
NM_001270448.1:c.1725C= NP_001257377.1:p.Asn575=
XM_006721516.2:c.1974C= XP_006721579.2:p.Asn658=
XM_011523829.1:c.1872C= XP_011522131.1:p.Asn624=
XM_011523830.1:c.1851C= XP_011522132.1:p.Asn617=
XR_934021.1:n.2056C=
XR_934022.1:n.1962C=
XR_934023.1:n.1983C=
XM_006721516.3:c.1974C= XP_006721579.2:p.Asn658=
XM_011523829.2:c.1872C= XP_011522131.1:p.Asn624=
XM_011523830.2:c.1851C= XP_011522132.1:p.Asn617=
XM_024450741.1:c.1941C= XP_024306509.1:p.Asn647=
XR_934021.2:n.2008C=
XR_934022.2:n.1914C=
XR_934023.2:n.1935C=
NM_000018.4:c.1953C= MANE Select NP_000009.1:p.Asn651=
NM_001033859.3:c.1887C= NP_001029031.1:p.Asn629=
NM_001270447.2:c.2022C= NP_001257376.1:p.Asn674=
NM_001270448.2:c.1725C= NP_001257377.1:p.Asn575=