Canonical Allele Identifier: CA2245699310
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221023A= , CM000679.2:g.7221023A= GRCh38
NC_000017.10:g.7124342A= , CM000679.1:g.7124342A= GRCh37
NC_000017.9:g.7065066A= NCBI36
NG_007975.1:g.6190A=
NG_008391.2:g.4028T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.442A= MANE Select ENSP00000349297.5:p.Ser148=
ENST00000322910.9:c.*397A= ENSP00000325395.5:n.*397A=
ENST00000350303.9:c.376A= ENSP00000344152.5:p.Ser126=
ENST00000356839.9:c.442A= ENSP00000349297.5:p.Ser148=
ENST00000543245.6:c.511A= ENSP00000438689.2:p.Ser171=
ENST00000577191.5:n.519A=
ENST00000577433.5:n.650A=
ENST00000577857.5:n.293+193A=
ENST00000579286.5:n.623A=
ENST00000579886.2:c.280A= ENSP00000463246.1:p.Ser94=
ENST00000580365.1:n.173A=
ENST00000581378.5:c.141A=
ENST00000581562.5:n.489A=
ENST00000582056.5:n.625A=
ENST00000582166.1:n.423A=
ENST00000583312.5:c.442A= ENSP00000467920.1:p.Ser148=
NM_000018.3:c.442A= NP_000009.1:p.Ser148=
NM_001033859.2:c.376A= NP_001029031.1:p.Ser126=
NM_001270447.1:c.511A= NP_001257376.1:p.Ser171=
NM_001270448.1:c.214A= NP_001257377.1:p.Ser72=
XM_006721516.2:c.442A= XP_006721579.2:p.Ser148=
XM_011523829.1:c.442A= XP_011522131.1:p.Ser148=
XM_011523830.1:c.442A= XP_011522132.1:p.Ser148=
XR_934021.1:n.549A=
XR_934022.1:n.549A=
XR_934023.1:n.549A=
XM_006721516.3:c.442A= XP_006721579.2:p.Ser148=
XM_011523829.2:c.442A= XP_011522131.1:p.Ser148=
XM_011523830.2:c.442A= XP_011522132.1:p.Ser148=
XM_024450741.1:c.442A= XP_024306509.1:p.Ser148=
XR_934021.2:n.501A=
XR_934022.2:n.501A=
XR_934023.2:n.501A=
NM_000018.4:c.442A= MANE Select NP_000009.1:p.Ser148=
NM_001033859.3:c.376A= NP_001029031.1:p.Ser126=
NM_001270447.2:c.511A= NP_001257376.1:p.Ser171=
NM_001270448.2:c.214A= NP_001257377.1:p.Ser72=