Canonical Allele Identifier: CA2245712861
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224074_7224076delinsGAC , CM000679.2:g.7224074_7224076delinsGAC GRCh38
NC_000017.10:g.7127393_7127395delinsGAC , CM000679.1:g.7127393_7127395delinsGAC GRCh37
NC_000017.9:g.7068117_7068119delinsGAC NCBI36
NG_007975.1:g.9241_9243delinsGAC
NG_008391.2:g.975_977delinsGTC
NG_033038.1:g.15469_15471delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1434+5_1434+7delinsGAC MANE Select ENSP00000349297.5:n.1434+5_1434+7delinsGAC
ENST00000322910.9:c.*1389+5_*1389+7delinsGAC ENSP00000325395.5:n.*1389+5_*1389+7delinsGAC
ENST00000350303.9:c.1368+5_1368+7delinsGAC ENSP00000344152.5:n.1368+5_1368+7delinsGAC
ENST00000356839.9:c.1434+5_1434+7delinsGAC ENSP00000349297.5:n.1434+5_1434+7delinsGAC
ENST00000542255.6:c.292+5_292+7delinsGAC
ENST00000543245.6:c.1503+5_1503+7delinsGAC ENSP00000438689.2:n.1503+5_1503+7delinsGAC
ENST00000578711.1:n.570_572delinsGAC
ENST00000579425.5:n.550+5_550+7delinsGAC
ENST00000579546.1:c.271+5_271+7delinsGAC
ENST00000579894.5:n.150_152delinsGAC
ENST00000583074.5:n.153+5_153+7delinsGAC
ENST00000583850.5:n.209+5_209+7delinsGAC
ENST00000583858.5:c.463+5_463+7delinsGAC
ENST00000585203.6:n.625+5_625+7delinsGAC
NM_000018.3:c.1434+5_1434+7delinsGAC NP_000009.1:n.1434+5_1434+7delinsGAC
NM_001033859.2:c.1368+5_1368+7delinsGAC NP_001029031.1:n.1368+5_1368+7delinsGAC
NM_001270447.1:c.1503+5_1503+7delinsGAC NP_001257376.1:n.1503+5_1503+7delinsGAC
NM_001270448.1:c.1206+5_1206+7delinsGAC NP_001257377.1:n.1206+5_1206+7delinsGAC
XM_006721516.2:c.1434+5_1434+7delinsGAC XP_006721579.2:n.1434+5_1434+7delinsGAC
XM_011523829.1:c.1434+5_1434+7delinsGAC XP_011522131.1:n.1434+5_1434+7delinsGAC
XM_011523830.1:c.1434+5_1434+7delinsGAC XP_011522132.1:n.1434+5_1434+7delinsGAC
XR_934021.1:n.1541+5_1541+7delinsGAC
XR_934022.1:n.1541+5_1541+7delinsGAC
XR_934023.1:n.1541+5_1541+7delinsGAC
XM_006721516.3:c.1434+5_1434+7delinsGAC XP_006721579.2:n.1434+5_1434+7delinsGAC
XM_011523829.2:c.1434+5_1434+7delinsGAC XP_011522131.1:n.1434+5_1434+7delinsGAC
XM_011523830.2:c.1434+5_1434+7delinsGAC XP_011522132.1:n.1434+5_1434+7delinsGAC
XM_024450741.1:c.1434+5_1434+7delinsGAC XP_024306509.1:n.1434+5_1434+7delinsGAC
XR_934021.2:n.1493+5_1493+7delinsGAC
XR_934022.2:n.1493+5_1493+7delinsGAC
XR_934023.2:n.1493+5_1493+7delinsGAC
NM_000018.4:c.1434+5_1434+7delinsGAC MANE Select NP_000009.1:n.1434+5_1434+7delinsGAC
NM_001033859.3:c.1368+5_1368+7delinsGAC NP_001029031.1:n.1368+5_1368+7delinsGAC
NM_001270447.2:c.1503+5_1503+7delinsGAC NP_001257376.1:n.1503+5_1503+7delinsGAC
NM_001270448.2:c.1206+5_1206+7delinsGAC NP_001257377.1:n.1206+5_1206+7delinsGAC