Canonical Allele Identifier: CA2245710011
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1057516686
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222866del , CM000679.2:g.7222866del GRCh38
NC_000017.10:g.7126185del , CM000679.1:g.7126185del GRCh37
NC_000017.9:g.7066909del NCBI36
NG_007975.1:g.8033del
NG_008391.2:g.2186del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1077+1del
ENST00000322910.9:c.*1032+1del
ENST00000350303.9:c.1011+1del
ENST00000356839.9:c.1077+1del
ENST00000543245.6:c.1146+1del
ENST00000578824.5:n.227del
ENST00000582379.1:n.462del
ENST00000583858.5:c.106+1del
ENST00000585203.6:n.19del
NM_000018.3:c.1077+1del
NM_001033859.2:c.1011+1del
NM_001270447.1:c.1146+1del
NM_001270448.1:c.849+1del
XM_006721516.2:c.1077+1del
XM_011523829.1:c.1077+1del
XM_011523830.1:c.1077+1del
XR_934021.1:n.1184+1del
XR_934022.1:n.1184+1del
XR_934023.1:n.1184+1del
XM_006721516.3:c.1077+1del
XM_011523829.2:c.1077+1del
XM_011523830.2:c.1077+1del
XM_024450741.1:c.1077+1del
XR_934021.2:n.1136+1del
XR_934022.2:n.1136+1del
XR_934023.2:n.1136+1del
NM_000018.4:c.1077+1del
NM_001033859.3:c.1011+1del
NM_001270447.2:c.1146+1del
NM_001270448.2:c.849+1del
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