Canonical Allele Identifier: CA2245716604
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225094C= , CM000679.2:g.7225094C= GRCh38
NC_000017.10:g.7128413C= , CM000679.1:g.7128413C= GRCh37
NC_000017.9:g.7069137C= NCBI36
NG_007975.1:g.10261C=
NG_033038.1:g.14451G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1965C= MANE Select ENSP00000349297.5:p.Phe655=
ENST00000322910.9:c.*1920C= ENSP00000325395.5:n.*1920C=
ENST00000350303.9:c.1899C= ENSP00000344152.5:p.Phe633=
ENST00000356839.9:c.1965C= ENSP00000349297.5:p.Phe655=
ENST00000542255.6:c.844C=
ENST00000543245.6:c.2034C= ENSP00000438689.2:p.Phe678=
ENST00000578033.1:n.390C=
ENST00000578319.5:n.546C=
ENST00000578711.1:n.1590C=
ENST00000578809.5:n.537C=
ENST00000579425.5:n.1081C=
ENST00000583848.5:c.331C= ENSP00000466487.1:n.331C=
ENST00000583850.5:n.736C=
ENST00000583858.5:c.896C=
NM_000018.3:c.1965C= NP_000009.1:p.Phe655=
NM_001033859.2:c.1899C= NP_001029031.1:p.Phe633=
NM_001270447.1:c.2034C= NP_001257376.1:p.Phe678=
NM_001270448.1:c.1737C= NP_001257377.1:p.Phe579=
XM_006721516.2:c.1986C= XP_006721579.2:p.Phe662=
XM_011523829.1:c.1884C= XP_011522131.1:p.Phe628=
XM_011523830.1:c.1863C= XP_011522132.1:p.Phe621=
XR_934021.1:n.2068C=
XR_934022.1:n.1974C=
XR_934023.1:n.1995C=
XM_006721516.3:c.1986C= XP_006721579.2:p.Phe662=
XM_011523829.2:c.1884C= XP_011522131.1:p.Phe628=
XM_011523830.2:c.1863C= XP_011522132.1:p.Phe621=
XM_024450741.1:c.1953C= XP_024306509.1:p.Phe651=
XR_934021.2:n.2020C=
XR_934022.2:n.1926C=
XR_934023.2:n.1947C=
NM_000018.4:c.1965C= MANE Select NP_000009.1:p.Phe655=
NM_001033859.3:c.1899C= NP_001029031.1:p.Phe633=
NM_001270447.2:c.2034C= NP_001257376.1:p.Phe678=
NM_001270448.2:c.1737C= NP_001257377.1:p.Phe579=