Canonical Allele Identifier: CA2245709978
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222855T= , CM000679.2:g.7222855T= GRCh38
NC_000017.10:g.7126174T= , CM000679.1:g.7126174T= GRCh37
NC_000017.9:g.7066898T= NCBI36
NG_007975.1:g.8022T=
NG_008391.2:g.2196A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1067T= MANE Select ENSP00000349297.5:p.Ile356=
ENST00000322910.9:c.*1022T= ENSP00000325395.5:n.*1022T=
ENST00000350303.9:c.1001T= ENSP00000344152.5:p.Ile334=
ENST00000356839.9:c.1067T= ENSP00000349297.5:p.Ile356=
ENST00000543245.6:c.1136T= ENSP00000438689.2:p.Ile379=
ENST00000578824.5:n.216T=
ENST00000582379.1:n.451T=
ENST00000583858.5:c.96T=
ENST00000585203.6:n.8T=
NM_000018.3:c.1067T= NP_000009.1:p.Ile356=
NM_001033859.2:c.1001T= NP_001029031.1:p.Ile334=
NM_001270447.1:c.1136T= NP_001257376.1:p.Ile379=
NM_001270448.1:c.839T= NP_001257377.1:p.Ile280=
XM_006721516.2:c.1067T= XP_006721579.2:p.Ile356=
XM_011523829.1:c.1067T= XP_011522131.1:p.Ile356=
XM_011523830.1:c.1067T= XP_011522132.1:p.Ile356=
XR_934021.1:n.1174T=
XR_934022.1:n.1174T=
XR_934023.1:n.1174T=
XM_006721516.3:c.1067T= XP_006721579.2:p.Ile356=
XM_011523829.2:c.1067T= XP_011522131.1:p.Ile356=
XM_011523830.2:c.1067T= XP_011522132.1:p.Ile356=
XM_024450741.1:c.1067T= XP_024306509.1:p.Ile356=
XR_934021.2:n.1126T=
XR_934022.2:n.1126T=
XR_934023.2:n.1126T=
NM_000018.4:c.1067T= MANE Select NP_000009.1:p.Ile356=
NM_001033859.3:c.1001T= NP_001029031.1:p.Ile334=
NM_001270447.2:c.1136T= NP_001257376.1:p.Ile379=
NM_001270448.2:c.839T= NP_001257377.1:p.Ile280=