Canonical Allele Identifier: CA2245716428
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225054T= , CM000679.2:g.7225054T= GRCh38
NC_000017.10:g.7128373T= , CM000679.1:g.7128373T= GRCh37
NC_000017.9:g.7069097T= NCBI36
NG_007975.1:g.10221T=
NG_033038.1:g.14491A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1925T= MANE Select ENSP00000349297.5:p.Val642=
ENST00000322910.9:c.*1880T= ENSP00000325395.5:n.*1880T=
ENST00000350303.9:c.1859T= ENSP00000344152.5:p.Val620=
ENST00000356839.9:c.1925T= ENSP00000349297.5:p.Val642=
ENST00000542255.6:c.804T=
ENST00000543245.6:c.1994T= ENSP00000438689.2:p.Val665=
ENST00000578033.1:n.350T=
ENST00000578319.5:n.506T=
ENST00000578711.1:n.1550T=
ENST00000578809.5:n.497T=
ENST00000579425.5:n.1041T=
ENST00000583848.5:c.291T= ENSP00000466487.1:n.291T=
ENST00000583850.5:n.696T=
ENST00000583858.5:c.856T=
NM_000018.3:c.1925T= NP_000009.1:p.Val642=
NM_001033859.2:c.1859T= NP_001029031.1:p.Val620=
NM_001270447.1:c.1994T= NP_001257376.1:p.Val665=
NM_001270448.1:c.1697T= NP_001257377.1:p.Val566=
XM_006721516.2:c.1946T= XP_006721579.2:p.Val649=
XM_011523829.1:c.1844T= XP_011522131.1:p.Val615=
XM_011523830.1:c.1823T= XP_011522132.1:p.Val608=
XR_934021.1:n.2028T=
XR_934022.1:n.1934T=
XR_934023.1:n.1955T=
XM_006721516.3:c.1946T= XP_006721579.2:p.Val649=
XM_011523829.2:c.1844T= XP_011522131.1:p.Val615=
XM_011523830.2:c.1823T= XP_011522132.1:p.Val608=
XM_024450741.1:c.1913T= XP_024306509.1:p.Val638=
XR_934021.2:n.1980T=
XR_934022.2:n.1886T=
XR_934023.2:n.1907T=
NM_000018.4:c.1925T= MANE Select NP_000009.1:p.Val642=
NM_001033859.3:c.1859T= NP_001029031.1:p.Val620=
NM_001270447.2:c.1994T= NP_001257376.1:p.Val665=
NM_001270448.2:c.1697T= NP_001257377.1:p.Val566=