Canonical Allele Identifier: CA2245710128
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222915_7222916delinsTC , CM000679.2:g.7222915_7222916delinsTC GRCh38
NC_000017.10:g.7126234_7126235delinsTC , CM000679.1:g.7126234_7126235delinsTC GRCh37
NC_000017.9:g.7066958_7066959delinsTC NCBI36
NG_007975.1:g.8082_8083delinsTC
NG_008391.2:g.2135_2136delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1077+50_1077+51delinsTC MANE Select ENSP00000349297.5:n.1077+50_1077+51delinsTC
ENST00000322910.9:c.*1032+50_*1032+51delinsTC ENSP00000325395.5:n.*1032+50_*1032+51delinsTC
ENST00000350303.9:c.1011+50_1011+51delinsTC ENSP00000344152.5:n.1011+50_1011+51delinsTC
ENST00000356839.9:c.1077+50_1077+51delinsTC ENSP00000349297.5:n.1077+50_1077+51delinsTC
ENST00000543245.6:c.1146+50_1146+51delinsTC ENSP00000438689.2:n.1146+50_1146+51delinsTC
ENST00000578824.5:n.276_277delinsTC
ENST00000582379.1:n.511_512delinsTC
ENST00000583858.5:c.106+50_106+51delinsTC
ENST00000585203.6:n.68_69delinsTC
NM_000018.3:c.1077+50_1077+51delinsTC NP_000009.1:n.1077+50_1077+51delinsTC
NM_001033859.2:c.1011+50_1011+51delinsTC NP_001029031.1:n.1011+50_1011+51delinsTC
NM_001270447.1:c.1146+50_1146+51delinsTC NP_001257376.1:n.1146+50_1146+51delinsTC
NM_001270448.1:c.849+50_849+51delinsTC NP_001257377.1:n.849+50_849+51delinsTC
XM_006721516.2:c.1077+50_1077+51delinsTC XP_006721579.2:n.1077+50_1077+51delinsTC
XM_011523829.1:c.1077+50_1077+51delinsTC XP_011522131.1:n.1077+50_1077+51delinsTC
XM_011523830.1:c.1077+50_1077+51delinsTC XP_011522132.1:n.1077+50_1077+51delinsTC
XR_934021.1:n.1184+50_1184+51delinsTC
XR_934022.1:n.1184+50_1184+51delinsTC
XR_934023.1:n.1184+50_1184+51delinsTC
XM_006721516.3:c.1077+50_1077+51delinsTC XP_006721579.2:n.1077+50_1077+51delinsTC
XM_011523829.2:c.1077+50_1077+51delinsTC XP_011522131.1:n.1077+50_1077+51delinsTC
XM_011523830.2:c.1077+50_1077+51delinsTC XP_011522132.1:n.1077+50_1077+51delinsTC
XM_024450741.1:c.1077+50_1077+51delinsTC XP_024306509.1:n.1077+50_1077+51delinsTC
XR_934021.2:n.1136+50_1136+51delinsTC
XR_934022.2:n.1136+50_1136+51delinsTC
XR_934023.2:n.1136+50_1136+51delinsTC
NM_000018.4:c.1077+50_1077+51delinsTC MANE Select NP_000009.1:n.1077+50_1077+51delinsTC
NM_001033859.3:c.1011+50_1011+51delinsTC NP_001029031.1:n.1011+50_1011+51delinsTC
NM_001270447.2:c.1146+50_1146+51delinsTC NP_001257376.1:n.1146+50_1146+51delinsTC
NM_001270448.2:c.849+50_849+51delinsTC NP_001257377.1:n.849+50_849+51delinsTC