Canonical Allele Identifier: CA981152823
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071239275

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221757_7221761del , CM000679.2:g.7221757_7221761del GRCh38
NC_000017.10:g.7125076_7125080del , CM000679.1:g.7125076_7125080del GRCh37
NC_000017.9:g.7065800_7065804del NCBI36
NG_007975.1:g.6924_6928del
NG_008391.2:g.3293_3297del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.622+75_622+79del MANE Select ENSP00000349297.5:n.622+75_622+79del
ENST00000322910.9:c.*577+75_*577+79del ENSP00000325395.5:n.*577+75_*577+79del
ENST00000350303.9:c.556+75_556+79del ENSP00000344152.5:n.556+75_556+79del
ENST00000356839.9:c.622+75_622+79del ENSP00000349297.5:n.622+75_622+79del
ENST00000543245.6:c.691+75_691+79del ENSP00000438689.2:n.691+75_691+79del
ENST00000577191.5:n.699+75_699+79del
ENST00000577857.5:n.438+75_438+79del
ENST00000579286.5:n.803+75_803+79del
ENST00000579886.2:c.460+75_460+79del ENSP00000463246.1:n.460+75_460+79del
ENST00000580365.1:n.353+75_353+79del
ENST00000581378.5:c.340+75_340+79del
ENST00000581562.5:n.525-195_525-191del
ENST00000583312.5:c.622+75_622+79del ENSP00000467920.1:n.622+75_622+79del
ENST00000583760.1:n.404+75_404+79del
NM_000018.3:c.622+75_622+79del NP_000009.1:n.622+75_622+79del
NM_001033859.2:c.556+75_556+79del NP_001029031.1:n.556+75_556+79del
NM_001270447.1:c.691+75_691+79del NP_001257376.1:n.691+75_691+79del
NM_001270448.1:c.394+75_394+79del NP_001257377.1:n.394+75_394+79del
XM_006721516.2:c.622+75_622+79del XP_006721579.2:n.622+75_622+79del
XM_011523829.1:c.622+75_622+79del XP_011522131.1:n.622+75_622+79del
XM_011523830.1:c.622+75_622+79del XP_011522132.1:n.622+75_622+79del
XR_934021.1:n.729+75_729+79del
XR_934022.1:n.729+75_729+79del
XR_934023.1:n.729+75_729+79del
XM_006721516.3:c.622+75_622+79del XP_006721579.2:n.622+75_622+79del
XM_011523829.2:c.622+75_622+79del XP_011522131.1:n.622+75_622+79del
XM_011523830.2:c.622+75_622+79del XP_011522132.1:n.622+75_622+79del
XM_024450741.1:c.622+75_622+79del XP_024306509.1:n.622+75_622+79del
XR_934021.2:n.681+75_681+79del
XR_934022.2:n.681+75_681+79del
XR_934023.2:n.681+75_681+79del
NM_000018.4:c.622+75_622+79del MANE Select NP_000009.1:n.622+75_622+79del
NM_001033859.3:c.556+75_556+79del NP_001029031.1:n.556+75_556+79del
NM_001270447.2:c.691+75_691+79del NP_001257376.1:n.691+75_691+79del
NM_001270448.2:c.394+75_394+79del NP_001257377.1:n.394+75_394+79del