Canonical Allele Identifier: CA1139533035
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222202_7222203dup , CM000679.2:g.7222202_7222203dup GRCh38
NC_000017.10:g.7125521_7125522dup , CM000679.1:g.7125521_7125522dup GRCh37
NC_000017.9:g.7066245_7066246dup NCBI36
NG_007975.1:g.7369_7370dup
NG_008391.2:g.2849_2850dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.778_779dup MANE Select ENSP00000349297.5:p.Val261ArgfsTer16
ENST00000322910.9:c.*733_*734dup ENSP00000325395.5:n.*733_*734dup
ENST00000350303.9:c.712_713dup ENSP00000344152.5:p.Val239ArgfsTer16
ENST00000356839.9:c.778_779dup ENSP00000349297.5:p.Val261ArgfsTer16
ENST00000543245.6:c.847_848dup ENSP00000438689.2:p.Val284ArgfsTer16
ENST00000577191.5:n.950_951dup
ENST00000581378.5:c.496_497dup
ENST00000582379.1:n.162_163dup
NM_000018.3:c.778_779dup NP_000009.1:p.Val261ArgfsTer16
NM_001033859.2:c.712_713dup NP_001029031.1:p.Val239ArgfsTer16
NM_001270447.1:c.847_848dup NP_001257376.1:p.Val284ArgfsTer16
NM_001270448.1:c.550_551dup NP_001257377.1:p.Val185ArgfsTer16
XM_006721516.2:c.778_779dup XP_006721579.2:p.Val261ArgfsTer16
XM_011523829.1:c.778_779dup XP_011522131.1:p.Val261ArgfsTer16
XM_011523830.1:c.778_779dup XP_011522132.1:p.Val261ArgfsTer16
XR_934021.1:n.885_886dup
XR_934022.1:n.885_886dup
XR_934023.1:n.885_886dup
XM_006721516.3:c.778_779dup XP_006721579.2:p.Val261ArgfsTer16
XM_011523829.2:c.778_779dup XP_011522131.1:p.Val261ArgfsTer16
XM_011523830.2:c.778_779dup XP_011522132.1:p.Val261ArgfsTer16
XM_024450741.1:c.778_779dup XP_024306509.1:p.Val261ArgfsTer16
XR_934021.2:n.837_838dup
XR_934022.2:n.837_838dup
XR_934023.2:n.837_838dup
NM_000018.4:c.778_779dup MANE Select NP_000009.1:p.Val261ArgfsTer16
NM_001033859.3:c.712_713dup NP_001029031.1:p.Val239ArgfsTer16
NM_001270447.2:c.847_848dup NP_001257376.1:p.Val284ArgfsTer16
NM_001270448.2:c.550_551dup NP_001257377.1:p.Val185ArgfsTer16