Canonical Allele Identifier: CA8337697
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 422995
dbSNP Id: rs758144859

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221009_7221048del , CM000679.2:g.7221009_7221048del GRCh38
NC_000017.10:g.7124328_7124367del , CM000679.1:g.7124328_7124367del GRCh37
NC_000017.9:g.7065052_7065091del NCBI36
NG_007975.1:g.6176_6215del
NG_008391.2:g.4012_4051del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.428_467del MANE Select ENSP00000349297.5:p.Gly143AlafsTer?
ENST00000322910.9:c.*383_*422del ENSP00000325395.5:n.*383_*422del
ENST00000350303.9:c.362_401del ENSP00000344152.5:p.Gly121AlafsTer?
ENST00000356839.9:c.428_467del ENSP00000349297.5:p.Gly143AlafsTer?
ENST00000543245.6:c.497_536del ENSP00000438689.2:p.Gly166AlafsTer?
ENST00000577191.5:n.505_544del
ENST00000577433.5:n.636_675del
ENST00000577857.5:n.293+179_293+218del
ENST00000579286.5:n.609_648del
ENST00000579886.2:c.266_305del ENSP00000463246.1:p.Gly89AlafsTer?
ENST00000580365.1:n.159_198del
ENST00000581378.5:c.127_166del
ENST00000581562.5:n.475_514del
ENST00000582056.5:n.611_650del
ENST00000582166.1:n.409_448del
ENST00000583312.5:c.428_467del ENSP00000467920.1:p.Gly143AlafsTer?
NM_000018.3:c.428_467del NP_000009.1:p.Gly143AlafsTer?
NM_001033859.2:c.362_401del NP_001029031.1:p.Gly121AlafsTer?
NM_001270447.1:c.497_536del NP_001257376.1:p.Gly166AlafsTer?
NM_001270448.1:c.200_239del NP_001257377.1:p.Gly67AlafsTer?
XM_006721516.2:c.428_467del XP_006721579.2:p.Gly143AlafsTer?
XM_011523829.1:c.428_467del XP_011522131.1:p.Gly143AlafsTer?
XM_011523830.1:c.428_467del XP_011522132.1:p.Gly143AlafsTer?
XR_934021.1:n.535_574del
XR_934022.1:n.535_574del
XR_934023.1:n.535_574del
XM_006721516.3:c.428_467del XP_006721579.2:p.Gly143AlafsTer?
XM_011523829.2:c.428_467del XP_011522131.1:p.Gly143AlafsTer?
XM_011523830.2:c.428_467del XP_011522132.1:p.Gly143AlafsTer?
XM_024450741.1:c.428_467del XP_024306509.1:p.Gly143AlafsTer?
XR_934021.2:n.487_526del
XR_934022.2:n.487_526del
XR_934023.2:n.487_526del
NM_000018.4:c.428_467del MANE Select NP_000009.1:p.Gly143AlafsTer?
NM_001033859.3:c.362_401del NP_001029031.1:p.Gly121AlafsTer?
NM_001270447.2:c.497_536del NP_001257376.1:p.Gly166AlafsTer?
NM_001270448.2:c.200_239del NP_001257377.1:p.Gly67AlafsTer?