Canonical Allele Identifier: CA774741614
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1474926523

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221302_7221304del , CM000679.2:g.7221302_7221304del GRCh38
NC_000017.10:g.7124621_7124623del , CM000679.1:g.7124621_7124623del GRCh37
NC_000017.9:g.7065345_7065347del NCBI36
NG_007975.1:g.6469_6471del
NG_008391.2:g.3748_3750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-236_478-234del MANE Select ENSP00000349297.5:n.478-236_478-234del
ENST00000322910.9:c.*433-236_*433-234del ENSP00000325395.5:n.*433-236_*433-234del
ENST00000350303.9:c.412-236_412-234del ENSP00000344152.5:n.412-236_412-234del
ENST00000356839.9:c.478-236_478-234del ENSP00000349297.5:n.478-236_478-234del
ENST00000543245.6:c.547-236_547-234del ENSP00000438689.2:n.547-236_547-234del
ENST00000577191.5:n.555-236_555-234del
ENST00000577433.5:n.686-236_686-234del
ENST00000577857.5:n.294-236_294-234del
ENST00000579286.5:n.659-236_659-234del
ENST00000579886.2:c.316-236_316-234del ENSP00000463246.1:n.316-236_316-234del
ENST00000580365.1:n.209-236_209-234del
ENST00000581378.5:c.177-217_177-215del
ENST00000581562.5:n.524+244_524+246del
ENST00000582166.1:n.459-236_459-234del
ENST00000583312.5:c.478-236_478-234del ENSP00000467920.1:n.478-236_478-234del
ENST00000583760.1:n.24_26del
NM_000018.3:c.478-236_478-234del NP_000009.1:n.478-236_478-234del
NM_001033859.2:c.412-236_412-234del NP_001029031.1:n.412-236_412-234del
NM_001270447.1:c.547-236_547-234del NP_001257376.1:n.547-236_547-234del
NM_001270448.1:c.250-236_250-234del NP_001257377.1:n.250-236_250-234del
XM_006721516.2:c.478-236_478-234del XP_006721579.2:n.478-236_478-234del
XM_011523829.1:c.478-236_478-234del XP_011522131.1:n.478-236_478-234del
XM_011523830.1:c.478-236_478-234del XP_011522132.1:n.478-236_478-234del
XR_934021.1:n.585-236_585-234del
XR_934022.1:n.585-236_585-234del
XR_934023.1:n.585-236_585-234del
XM_006721516.3:c.478-236_478-234del XP_006721579.2:n.478-236_478-234del
XM_011523829.2:c.478-236_478-234del XP_011522131.1:n.478-236_478-234del
XM_011523830.2:c.478-236_478-234del XP_011522132.1:n.478-236_478-234del
XM_024450741.1:c.478-236_478-234del XP_024306509.1:n.478-236_478-234del
XR_934021.2:n.537-236_537-234del
XR_934022.2:n.537-236_537-234del
XR_934023.2:n.537-236_537-234del
NM_000018.4:c.478-236_478-234del MANE Select NP_000009.1:n.478-236_478-234del
NM_001033859.3:c.412-236_412-234del NP_001029031.1:n.412-236_412-234del
NM_001270447.2:c.547-236_547-234del NP_001257376.1:n.547-236_547-234del
NM_001270448.2:c.250-236_250-234del NP_001257377.1:n.250-236_250-234del