Canonical Allele Identifier: CA2245701949
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222415_7222419delinsCTGAA , CM000679.2:g.7222415_7222419delinsCTGAA GRCh38
NC_000017.10:g.7125734_7125738delinsCTGAA , CM000679.1:g.7125734_7125738delinsCTGAA GRCh37
NC_000017.9:g.7066458_7066462delinsCTGAA NCBI36
NG_007975.1:g.7582_7586delinsCTGAA
NG_008391.2:g.2632_2636delinsTTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.878+113_878+117delinsCTGAA MANE Select ENSP00000349297.5:n.878+113_878+117delinsCTGAA
ENST00000322910.9:c.*833+113_*833+117delinsCTGAA ENSP00000325395.5:n.*833+113_*833+117delinsCTGAA
ENST00000350303.9:c.812+113_812+117delinsCTGAA ENSP00000344152.5:n.812+113_812+117delinsCTGAA
ENST00000356839.9:c.878+113_878+117delinsCTGAA ENSP00000349297.5:n.878+113_878+117delinsCTGAA
ENST00000543245.6:c.947+113_947+117delinsCTGAA ENSP00000438689.2:n.947+113_947+117delinsCTGAA
ENST00000577191.5:n.1163_1167delinsCTGAA
ENST00000581378.5:c.596+113_596+117delinsCTGAA
ENST00000582379.1:n.262+113_262+117delinsCTGAA
NM_000018.3:c.878+113_878+117delinsCTGAA NP_000009.1:n.878+113_878+117delinsCTGAA
NM_001033859.2:c.812+113_812+117delinsCTGAA NP_001029031.1:n.812+113_812+117delinsCTGAA
NM_001270447.1:c.947+113_947+117delinsCTGAA NP_001257376.1:n.947+113_947+117delinsCTGAA
NM_001270448.1:c.650+113_650+117delinsCTGAA NP_001257377.1:n.650+113_650+117delinsCTGAA
XM_006721516.2:c.878+113_878+117delinsCTGAA XP_006721579.2:n.878+113_878+117delinsCTGAA
XM_011523829.1:c.878+113_878+117delinsCTGAA XP_011522131.1:n.878+113_878+117delinsCTGAA
XM_011523830.1:c.878+113_878+117delinsCTGAA XP_011522132.1:n.878+113_878+117delinsCTGAA
XR_934021.1:n.985+113_985+117delinsCTGAA
XR_934022.1:n.985+113_985+117delinsCTGAA
XR_934023.1:n.985+113_985+117delinsCTGAA
XM_006721516.3:c.878+113_878+117delinsCTGAA XP_006721579.2:n.878+113_878+117delinsCTGAA
XM_011523829.2:c.878+113_878+117delinsCTGAA XP_011522131.1:n.878+113_878+117delinsCTGAA
XM_011523830.2:c.878+113_878+117delinsCTGAA XP_011522132.1:n.878+113_878+117delinsCTGAA
XM_024450741.1:c.878+113_878+117delinsCTGAA XP_024306509.1:n.878+113_878+117delinsCTGAA
XR_934021.2:n.937+113_937+117delinsCTGAA
XR_934022.2:n.937+113_937+117delinsCTGAA
XR_934023.2:n.937+113_937+117delinsCTGAA
NM_000018.4:c.878+113_878+117delinsCTGAA MANE Select NP_000009.1:n.878+113_878+117delinsCTGAA
NM_001033859.3:c.812+113_812+117delinsCTGAA NP_001029031.1:n.812+113_812+117delinsCTGAA
NM_001270447.2:c.947+113_947+117delinsCTGAA NP_001257376.1:n.947+113_947+117delinsCTGAA
NM_001270448.2:c.650+113_650+117delinsCTGAA NP_001257377.1:n.650+113_650+117delinsCTGAA