Canonical Allele Identifier: CA981153996
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071331165

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223491del , CM000679.2:g.7223491del GRCh38
NC_000017.10:g.7126810del , CM000679.1:g.7126810del GRCh37
NC_000017.9:g.7067534del NCBI36
NG_007975.1:g.8658del
NG_008391.2:g.1560del
NG_033038.1:g.16054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1183-153del MANE Select ENSP00000349297.5:n.1183-153del
ENST00000322910.9:c.*1138-153del ENSP00000325395.5:n.*1138-153del
ENST00000350303.9:c.1117-153del ENSP00000344152.5:n.1117-153del
ENST00000356839.9:c.1183-153del ENSP00000349297.5:n.1183-153del
ENST00000542255.6:c.41-153del
ENST00000543245.6:c.1252-153del ENSP00000438689.2:n.1252-153del
ENST00000578579.2:n.201del
ENST00000578824.5:n.599-153del
ENST00000579425.5:n.207-153del
ENST00000579546.1:c.20-153del
ENST00000583858.5:c.212-153del
ENST00000585203.6:n.391-153del
NM_000018.3:c.1183-153del NP_000009.1:n.1183-153del
NM_001033859.2:c.1117-153del NP_001029031.1:n.1117-153del
NM_001270447.1:c.1252-153del NP_001257376.1:n.1252-153del
NM_001270448.1:c.955-153del NP_001257377.1:n.955-153del
XM_006721516.2:c.1183-153del XP_006721579.2:n.1183-153del
XM_011523829.1:c.1183-153del XP_011522131.1:n.1183-153del
XM_011523830.1:c.1183-153del XP_011522132.1:n.1183-153del
XR_934021.1:n.1290-153del
XR_934022.1:n.1290-153del
XR_934023.1:n.1290-153del
XM_006721516.3:c.1183-153del XP_006721579.2:n.1183-153del
XM_011523829.2:c.1183-153del XP_011522131.1:n.1183-153del
XM_011523830.2:c.1183-153del XP_011522132.1:n.1183-153del
XM_024450741.1:c.1183-153del XP_024306509.1:n.1183-153del
XR_934021.2:n.1242-153del
XR_934022.2:n.1242-153del
XR_934023.2:n.1242-153del
NM_000018.4:c.1183-153del MANE Select NP_000009.1:n.1183-153del
NM_001033859.3:c.1117-153del NP_001029031.1:n.1117-153del
NM_001270447.2:c.1252-153del NP_001257376.1:n.1252-153del
NM_001270448.2:c.955-153del NP_001257377.1:n.955-153del