Canonical Allele Identifier: CA2245710142
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222918C= , CM000679.2:g.7222918C= GRCh38
NC_000017.10:g.7126237C= , CM000679.1:g.7126237C= GRCh37
NC_000017.9:g.7066961C= NCBI36
NG_007975.1:g.8085C=
NG_008391.2:g.2133G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1077+53C= MANE Select ENSP00000349297.5:n.1077+53C=
ENST00000322910.9:c.*1032+53C= ENSP00000325395.5:n.*1032+53C=
ENST00000350303.9:c.1011+53C= ENSP00000344152.5:n.1011+53C=
ENST00000356839.9:c.1077+53C= ENSP00000349297.5:n.1077+53C=
ENST00000543245.6:c.1146+53C= ENSP00000438689.2:n.1146+53C=
ENST00000578824.5:n.279C=
ENST00000582379.1:n.514C=
ENST00000583858.5:c.106+53C=
ENST00000585203.6:n.71C=
NM_000018.3:c.1077+53C= NP_000009.1:n.1077+53C=
NM_001033859.2:c.1011+53C= NP_001029031.1:n.1011+53C=
NM_001270447.1:c.1146+53C= NP_001257376.1:n.1146+53C=
NM_001270448.1:c.849+53C= NP_001257377.1:n.849+53C=
XM_006721516.2:c.1077+53C= XP_006721579.2:n.1077+53C=
XM_011523829.1:c.1077+53C= XP_011522131.1:n.1077+53C=
XM_011523830.1:c.1077+53C= XP_011522132.1:n.1077+53C=
XR_934021.1:n.1184+53C=
XR_934022.1:n.1184+53C=
XR_934023.1:n.1184+53C=
XM_006721516.3:c.1077+53C= XP_006721579.2:n.1077+53C=
XM_011523829.2:c.1077+53C= XP_011522131.1:n.1077+53C=
XM_011523830.2:c.1077+53C= XP_011522132.1:n.1077+53C=
XM_024450741.1:c.1077+53C= XP_024306509.1:n.1077+53C=
XR_934021.2:n.1136+53C=
XR_934022.2:n.1136+53C=
XR_934023.2:n.1136+53C=
NM_000018.4:c.1077+53C= MANE Select NP_000009.1:n.1077+53C=
NM_001033859.3:c.1011+53C= NP_001029031.1:n.1011+53C=
NM_001270447.2:c.1146+53C= NP_001257376.1:n.1146+53C=
NM_001270448.2:c.849+53C= NP_001257377.1:n.849+53C=