Canonical Allele Identifier: CA624860723
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1320370240

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224252del , CM000679.2:g.7224252del GRCh38
NC_000017.10:g.7127571del , CM000679.1:g.7127571del GRCh37
NC_000017.9:g.7068295del NCBI36
NG_007975.1:g.9419del
NG_008391.2:g.799del
NG_033038.1:g.15293del

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1532+9del MANE Select ENSP00000349297.5:n.1532+9del
ENST00000322910.9:c.*1487+9del ENSP00000325395.5:n.*1487+9del
ENST00000350303.9:c.1466+9del ENSP00000344152.5:n.1466+9del
ENST00000356839.9:c.1532+9del ENSP00000349297.5:n.1532+9del
ENST00000542255.6:c.390+9del
ENST00000543245.6:c.1601+9del ENSP00000438689.2:n.1601+9del
ENST00000578319.5:n.27+9del
ENST00000578711.1:n.748del
ENST00000578809.5:n.36del
ENST00000579391.1:n.140+9del
ENST00000579425.5:n.648+9del
ENST00000579546.1:c.272-69del
ENST00000579894.5:n.319+9del
ENST00000583074.5:n.154-69del
ENST00000583850.5:n.307+9del
ENST00000583858.5:c.464-69del
ENST00000585203.6:n.723+9del
NM_000018.3:c.1532+9del NP_000009.1:n.1532+9del
NM_001033859.2:c.1466+9del NP_001029031.1:n.1466+9del
NM_001270447.1:c.1601+9del NP_001257376.1:n.1601+9del
NM_001270448.1:c.1304+9del NP_001257377.1:n.1304+9del
XM_006721516.2:c.1532+9del XP_006721579.2:n.1532+9del
XM_011523829.1:c.1435-69del XP_011522131.1:n.1435-69del
XM_011523830.1:c.1435-69del XP_011522132.1:n.1435-69del
XR_934021.1:n.1639+9del
XR_934022.1:n.1542-69del
XR_934023.1:n.1542-69del
XM_006721516.3:c.1532+9del XP_006721579.2:n.1532+9del
XM_011523829.2:c.1435-69del XP_011522131.1:n.1435-69del
XM_011523830.2:c.1435-69del XP_011522132.1:n.1435-69del
XM_024450741.1:c.1435-69del XP_024306509.1:n.1435-69del
XR_934021.2:n.1591+9del
XR_934022.2:n.1494-69del
XR_934023.2:n.1494-69del
NM_000018.4:c.1532+9del MANE Select NP_000009.1:n.1532+9del
NM_001033859.3:c.1466+9del NP_001029031.1:n.1466+9del
NM_001270447.2:c.1601+9del NP_001257376.1:n.1601+9del
NM_001270448.2:c.1304+9del NP_001257377.1:n.1304+9del