Canonical Allele Identifier: CA2245715394
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224754C= , CM000679.2:g.7224754C= GRCh38
NC_000017.10:g.7128073C= , CM000679.1:g.7128073C= GRCh37
NC_000017.9:g.7068797C= NCBI36
NG_007975.1:g.9921C=
NG_008391.2:g.297G=
NG_033038.1:g.14791G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1751+40C= MANE Select ENSP00000349297.5:n.1751+40C=
ENST00000322910.9:c.*1706+40C= ENSP00000325395.5:n.*1706+40C=
ENST00000350303.9:c.1685+40C= ENSP00000344152.5:n.1685+40C=
ENST00000356839.9:c.1751+40C= ENSP00000349297.5:n.1751+40C=
ENST00000542255.6:c.576C=
ENST00000543245.6:c.1820+40C= ENSP00000438689.2:n.1820+40C=
ENST00000578033.1:n.122C=
ENST00000578319.5:n.332+40C=
ENST00000578711.1:n.1250C=
ENST00000578809.5:n.323+40C=
ENST00000579425.5:n.867+40C=
ENST00000579546.1:c.486+40C=
ENST00000583074.5:n.339C=
ENST00000583848.5:c.117+40C= ENSP00000466487.1:n.117+40C=
ENST00000583850.5:n.522+40C=
ENST00000583858.5:c.682+40C=
ENST00000585203.6:n.942+40C=
NM_000018.3:c.1751+40C= NP_000009.1:n.1751+40C=
NM_001033859.2:c.1685+40C= NP_001029031.1:n.1685+40C=
NM_001270447.1:c.1820+40C= NP_001257376.1:n.1820+40C=
NM_001270448.1:c.1523+40C= NP_001257377.1:n.1523+40C=
XM_006721516.2:c.1718C= XP_006721579.2:p.Pro573=
XM_011523829.1:c.1616C= XP_011522131.1:p.Pro539=
XM_011523830.1:c.1649+40C= XP_011522132.1:n.1649+40C=
XR_934021.1:n.1854+40C=
XR_934022.1:n.1760+40C=
XR_934023.1:n.1727C=
XM_006721516.3:c.1718C= XP_006721579.2:p.Pro573=
XM_011523829.2:c.1616C= XP_011522131.1:p.Pro539=
XM_011523830.2:c.1649+40C= XP_011522132.1:n.1649+40C=
XM_024450741.1:c.1739+40C= XP_024306509.1:n.1739+40C=
XR_934021.2:n.1806+40C=
XR_934022.2:n.1712+40C=
XR_934023.2:n.1679C=
NM_000018.4:c.1751+40C= MANE Select NP_000009.1:n.1751+40C=
NM_001033859.3:c.1685+40C= NP_001029031.1:n.1685+40C=
NM_001270447.2:c.1820+40C= NP_001257376.1:n.1820+40C=
NM_001270448.2:c.1523+40C= NP_001257377.1:n.1523+40C=