Canonical Allele Identifier: CA2245716590
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225093T= , CM000679.2:g.7225093T= GRCh38
NC_000017.10:g.7128412T= , CM000679.1:g.7128412T= GRCh37
NC_000017.9:g.7069136T= NCBI36
NG_007975.1:g.10260T=
NG_033038.1:g.14452A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1964T= MANE Select ENSP00000349297.5:p.Phe655=
ENST00000322910.9:c.*1919T= ENSP00000325395.5:n.*1919T=
ENST00000350303.9:c.1898T= ENSP00000344152.5:p.Phe633=
ENST00000356839.9:c.1964T= ENSP00000349297.5:p.Phe655=
ENST00000542255.6:c.843T=
ENST00000543245.6:c.2033T= ENSP00000438689.2:p.Phe678=
ENST00000578033.1:n.389T=
ENST00000578319.5:n.545T=
ENST00000578711.1:n.1589T=
ENST00000578809.5:n.536T=
ENST00000579425.5:n.1080T=
ENST00000583848.5:c.330T= ENSP00000466487.1:n.330T=
ENST00000583850.5:n.735T=
ENST00000583858.5:c.895T=
NM_000018.3:c.1964T= NP_000009.1:p.Phe655=
NM_001033859.2:c.1898T= NP_001029031.1:p.Phe633=
NM_001270447.1:c.2033T= NP_001257376.1:p.Phe678=
NM_001270448.1:c.1736T= NP_001257377.1:p.Phe579=
XM_006721516.2:c.1985T= XP_006721579.2:p.Phe662=
XM_011523829.1:c.1883T= XP_011522131.1:p.Phe628=
XM_011523830.1:c.1862T= XP_011522132.1:p.Phe621=
XR_934021.1:n.2067T=
XR_934022.1:n.1973T=
XR_934023.1:n.1994T=
XM_006721516.3:c.1985T= XP_006721579.2:p.Phe662=
XM_011523829.2:c.1883T= XP_011522131.1:p.Phe628=
XM_011523830.2:c.1862T= XP_011522132.1:p.Phe621=
XM_024450741.1:c.1952T= XP_024306509.1:p.Phe651=
XR_934021.2:n.2019T=
XR_934022.2:n.1925T=
XR_934023.2:n.1946T=
NM_000018.4:c.1964T= MANE Select NP_000009.1:p.Phe655=
NM_001033859.3:c.1898T= NP_001029031.1:p.Phe633=
NM_001270447.2:c.2033T= NP_001257376.1:p.Phe678=
NM_001270448.2:c.1736T= NP_001257377.1:p.Phe579=