Canonical Allele Identifier: CA2245699616
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221300_7221303delinsCAAT , CM000679.2:g.7221300_7221303delinsCAAT GRCh38
NC_000017.10:g.7124619_7124622delinsCAAT , CM000679.1:g.7124619_7124622delinsCAAT GRCh37
NC_000017.9:g.7065343_7065346delinsCAAT NCBI36
NG_007975.1:g.6467_6470delinsCAAT
NG_008391.2:g.3748_3751delinsATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-238_478-235delinsCAAT MANE Select ENSP00000349297.5:n.478-238_478-235delinsCAAT
ENST00000322910.9:c.*433-238_*433-235delinsCAAT ENSP00000325395.5:n.*433-238_*433-235delinsCAAT
ENST00000350303.9:c.412-238_412-235delinsCAAT ENSP00000344152.5:n.412-238_412-235delinsCAAT
ENST00000356839.9:c.478-238_478-235delinsCAAT ENSP00000349297.5:n.478-238_478-235delinsCAAT
ENST00000543245.6:c.547-238_547-235delinsCAAT ENSP00000438689.2:n.547-238_547-235delinsCAAT
ENST00000577191.5:n.555-238_555-235delinsCAAT
ENST00000577433.5:n.686-238_686-235delinsCAAT
ENST00000577857.5:n.294-238_294-235delinsCAAT
ENST00000579286.5:n.659-238_659-235delinsCAAT
ENST00000579886.2:c.316-238_316-235delinsCAAT ENSP00000463246.1:n.316-238_316-235delinsCAAT
ENST00000580365.1:n.209-238_209-235delinsCAAT
ENST00000581378.5:c.177-219_177-216delinsCAAT
ENST00000581562.5:n.524+242_524+245delinsCAAT
ENST00000582166.1:n.459-238_459-235delinsCAAT
ENST00000583312.5:c.478-238_478-235delinsCAAT ENSP00000467920.1:n.478-238_478-235delinsCAAT
ENST00000583760.1:n.22_25delinsCAAT
NM_000018.3:c.478-238_478-235delinsCAAT NP_000009.1:n.478-238_478-235delinsCAAT
NM_001033859.2:c.412-238_412-235delinsCAAT NP_001029031.1:n.412-238_412-235delinsCAAT
NM_001270447.1:c.547-238_547-235delinsCAAT NP_001257376.1:n.547-238_547-235delinsCAAT
NM_001270448.1:c.250-238_250-235delinsCAAT NP_001257377.1:n.250-238_250-235delinsCAAT
XM_006721516.2:c.478-238_478-235delinsCAAT XP_006721579.2:n.478-238_478-235delinsCAAT
XM_011523829.1:c.478-238_478-235delinsCAAT XP_011522131.1:n.478-238_478-235delinsCAAT
XM_011523830.1:c.478-238_478-235delinsCAAT XP_011522132.1:n.478-238_478-235delinsCAAT
XR_934021.1:n.585-238_585-235delinsCAAT
XR_934022.1:n.585-238_585-235delinsCAAT
XR_934023.1:n.585-238_585-235delinsCAAT
XM_006721516.3:c.478-238_478-235delinsCAAT XP_006721579.2:n.478-238_478-235delinsCAAT
XM_011523829.2:c.478-238_478-235delinsCAAT XP_011522131.1:n.478-238_478-235delinsCAAT
XM_011523830.2:c.478-238_478-235delinsCAAT XP_011522132.1:n.478-238_478-235delinsCAAT
XM_024450741.1:c.478-238_478-235delinsCAAT XP_024306509.1:n.478-238_478-235delinsCAAT
XR_934021.2:n.537-238_537-235delinsCAAT
XR_934022.2:n.537-238_537-235delinsCAAT
XR_934023.2:n.537-238_537-235delinsCAAT
NM_000018.4:c.478-238_478-235delinsCAAT MANE Select NP_000009.1:n.478-238_478-235delinsCAAT
NM_001033859.3:c.412-238_412-235delinsCAAT NP_001029031.1:n.412-238_412-235delinsCAAT
NM_001270447.2:c.547-238_547-235delinsCAAT NP_001257376.1:n.547-238_547-235delinsCAAT
NM_001270448.2:c.250-238_250-235delinsCAAT NP_001257377.1:n.250-238_250-235delinsCAAT