Canonical Allele Identifier: CA2245700825
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221973G= , CM000679.2:g.7221973G= GRCh38
NC_000017.10:g.7125292G= , CM000679.1:g.7125292G= GRCh37
NC_000017.9:g.7066016G= NCBI36
NG_007975.1:g.7140G=
NG_008391.2:g.3078C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.644G= MANE Select ENSP00000349297.5:p.Cys215=
ENST00000322910.9:c.*599G= ENSP00000325395.5:n.*599G=
ENST00000350303.9:c.578G= ENSP00000344152.5:p.Cys193=
ENST00000356839.9:c.644G= ENSP00000349297.5:p.Cys215=
ENST00000543245.6:c.713G= ENSP00000438689.2:p.Cys238=
ENST00000577191.5:n.721G=
ENST00000577857.5:n.460G=
ENST00000579286.5:n.825G=
ENST00000580365.1:n.375G=
ENST00000581378.5:c.362G=
ENST00000581562.5:n.546G=
ENST00000582379.1:n.28G=
ENST00000583312.5:c.659G= ENSP00000467920.1:p.Cys220=
ENST00000583760.1:n.426G=
NM_000018.3:c.644G= NP_000009.1:p.Cys215=
NM_001033859.2:c.578G= NP_001029031.1:p.Cys193=
NM_001270447.1:c.713G= NP_001257376.1:p.Cys238=
NM_001270448.1:c.416G= NP_001257377.1:p.Cys139=
XM_006721516.2:c.644G= XP_006721579.2:p.Cys215=
XM_011523829.1:c.644G= XP_011522131.1:p.Cys215=
XM_011523830.1:c.644G= XP_011522132.1:p.Cys215=
XR_934021.1:n.751G=
XR_934022.1:n.751G=
XR_934023.1:n.751G=
XM_006721516.3:c.644G= XP_006721579.2:p.Cys215=
XM_011523829.2:c.644G= XP_011522131.1:p.Cys215=
XM_011523830.2:c.644G= XP_011522132.1:p.Cys215=
XM_024450741.1:c.644G= XP_024306509.1:p.Cys215=
XR_934021.2:n.703G=
XR_934022.2:n.703G=
XR_934023.2:n.703G=
NM_000018.4:c.644G= MANE Select NP_000009.1:p.Cys215=
NM_001033859.3:c.578G= NP_001029031.1:p.Cys193=
NM_001270447.2:c.713G= NP_001257376.1:p.Cys238=
NM_001270448.2:c.416G= NP_001257377.1:p.Cys139=