Canonical Allele Identifier: CA1139770377
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224072_7224073del , CM000679.2:g.7224072_7224073del GRCh38
NC_000017.10:g.7127391_7127392del , CM000679.1:g.7127391_7127392del GRCh37
NC_000017.9:g.7068115_7068116del NCBI36
NG_007975.1:g.9239_9240del
NG_008391.2:g.978_979del
NG_033038.1:g.15472_15473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1434+3_1434+4del MANE Select ENSP00000349297.5:n.1434+3_1434+4del
ENST00000322910.9:c.*1389+3_*1389+4del ENSP00000325395.5:n.*1389+3_*1389+4del
ENST00000350303.9:c.1368+3_1368+4del ENSP00000344152.5:n.1368+3_1368+4del
ENST00000356839.9:c.1434+3_1434+4del ENSP00000349297.5:n.1434+3_1434+4del
ENST00000542255.6:c.292+3_292+4del
ENST00000543245.6:c.1503+3_1503+4del ENSP00000438689.2:n.1503+3_1503+4del
ENST00000578711.1:n.568_569del
ENST00000579425.5:n.550+3_550+4del
ENST00000579546.1:c.271+3_271+4del
ENST00000579894.5:n.148_149del
ENST00000583074.5:n.153+3_153+4del
ENST00000583850.5:n.209+3_209+4del
ENST00000583858.5:c.463+3_463+4del
ENST00000585203.6:n.625+3_625+4del
NM_000018.3:c.1434+3_1434+4del NP_000009.1:n.1434+3_1434+4del
NM_001033859.2:c.1368+3_1368+4del NP_001029031.1:n.1368+3_1368+4del
NM_001270447.1:c.1503+3_1503+4del NP_001257376.1:n.1503+3_1503+4del
NM_001270448.1:c.1206+3_1206+4del NP_001257377.1:n.1206+3_1206+4del
XM_006721516.2:c.1434+3_1434+4del XP_006721579.2:n.1434+3_1434+4del
XM_011523829.1:c.1434+3_1434+4del XP_011522131.1:n.1434+3_1434+4del
XM_011523830.1:c.1434+3_1434+4del XP_011522132.1:n.1434+3_1434+4del
XR_934021.1:n.1541+3_1541+4del
XR_934022.1:n.1541+3_1541+4del
XR_934023.1:n.1541+3_1541+4del
XM_006721516.3:c.1434+3_1434+4del XP_006721579.2:n.1434+3_1434+4del
XM_011523829.2:c.1434+3_1434+4del XP_011522131.1:n.1434+3_1434+4del
XM_011523830.2:c.1434+3_1434+4del XP_011522132.1:n.1434+3_1434+4del
XM_024450741.1:c.1434+3_1434+4del XP_024306509.1:n.1434+3_1434+4del
XR_934021.2:n.1493+3_1493+4del
XR_934022.2:n.1493+3_1493+4del
XR_934023.2:n.1493+3_1493+4del
NM_000018.4:c.1434+3_1434+4del MANE Select NP_000009.1:n.1434+3_1434+4del
NM_001033859.3:c.1368+3_1368+4del NP_001029031.1:n.1368+3_1368+4del
NM_001270447.2:c.1503+3_1503+4del NP_001257376.1:n.1503+3_1503+4del
NM_001270448.2:c.1206+3_1206+4del NP_001257377.1:n.1206+3_1206+4del