Canonical Allele Identifier: CA2808366089
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222904_7222905insCCCAACAC , CM000679.2:g.7222904_7222905insCCCAACAC GRCh38
NC_000017.10:g.7126223_7126224insCCCAACAC , CM000679.1:g.7126223_7126224insCCCAACAC GRCh37
NC_000017.9:g.7066947_7066948insCCCAACAC NCBI36
NG_007975.1:g.8071_8072insCCCAACAC
NG_008391.2:g.2146_2147insGTGTTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1077+39_1077+40insCCCAACAC MANE Select ENSP00000349297.5:n.1077+39_1077+40insCCCAACAC
ENST00000322910.9:c.*1032+39_*1032+40insCCCAACAC ENSP00000325395.5:n.*1032+39_*1032+40insCCCAACAC
ENST00000350303.9:c.1011+39_1011+40insCCCAACAC ENSP00000344152.5:n.1011+39_1011+40insCCCAACAC
ENST00000356839.9:c.1077+39_1077+40insCCCAACAC ENSP00000349297.5:n.1077+39_1077+40insCCCAACAC
ENST00000543245.6:c.1146+39_1146+40insCCCAACAC ENSP00000438689.2:n.1146+39_1146+40insCCCAACAC
ENST00000578824.5:n.265_266insCCCAACAC
ENST00000582379.1:n.500_501insCCCAACAC
ENST00000583858.5:c.106+39_106+40insCCCAACAC
ENST00000585203.6:n.57_58insCCCAACAC
NM_000018.3:c.1077+39_1077+40insCCCAACAC NP_000009.1:n.1077+39_1077+40insCCCAACAC
NM_001033859.2:c.1011+39_1011+40insCCCAACAC NP_001029031.1:n.1011+39_1011+40insCCCAACAC
NM_001270447.1:c.1146+39_1146+40insCCCAACAC NP_001257376.1:n.1146+39_1146+40insCCCAACAC
NM_001270448.1:c.849+39_849+40insCCCAACAC NP_001257377.1:n.849+39_849+40insCCCAACAC
XM_006721516.2:c.1077+39_1077+40insCCCAACAC XP_006721579.2:n.1077+39_1077+40insCCCAACAC
XM_011523829.1:c.1077+39_1077+40insCCCAACAC XP_011522131.1:n.1077+39_1077+40insCCCAACAC
XM_011523830.1:c.1077+39_1077+40insCCCAACAC XP_011522132.1:n.1077+39_1077+40insCCCAACAC
XR_934021.1:n.1184+39_1184+40insCCCAACAC
XR_934022.1:n.1184+39_1184+40insCCCAACAC
XR_934023.1:n.1184+39_1184+40insCCCAACAC
XM_006721516.3:c.1077+39_1077+40insCCCAACAC XP_006721579.2:n.1077+39_1077+40insCCCAACAC
XM_011523829.2:c.1077+39_1077+40insCCCAACAC XP_011522131.1:n.1077+39_1077+40insCCCAACAC
XM_011523830.2:c.1077+39_1077+40insCCCAACAC XP_011522132.1:n.1077+39_1077+40insCCCAACAC
XM_024450741.1:c.1077+39_1077+40insCCCAACAC XP_024306509.1:n.1077+39_1077+40insCCCAACAC
XR_934021.2:n.1136+39_1136+40insCCCAACAC
XR_934022.2:n.1136+39_1136+40insCCCAACAC
XR_934023.2:n.1136+39_1136+40insCCCAACAC
NM_000018.4:c.1077+39_1077+40insCCCAACAC MANE Select NP_000009.1:n.1077+39_1077+40insCCCAACAC
NM_001033859.3:c.1011+39_1011+40insCCCAACAC NP_001029031.1:n.1011+39_1011+40insCCCAACAC
NM_001270447.2:c.1146+39_1146+40insCCCAACAC NP_001257376.1:n.1146+39_1146+40insCCCAACAC
NM_001270448.2:c.849+39_849+40insCCCAACAC NP_001257377.1:n.849+39_849+40insCCCAACAC