Canonical Allele Identifier: CA2245699938
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221515_7221517delinsCCA , CM000679.2:g.7221515_7221517delinsCCA GRCh38
NC_000017.10:g.7124834_7124836delinsCCA , CM000679.1:g.7124834_7124836delinsCCA GRCh37
NC_000017.9:g.7065558_7065560delinsCCA NCBI36
NG_007975.1:g.6682_6684delinsCCA
NG_008391.2:g.3534_3536delinsTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.478-23_478-21delinsCCA MANE Select ENSP00000349297.5:n.478-23_478-21delinsCC...
ENST00000322910.9:c.*433-23_*433-21delinsCCA ENSP00000325395.5:n.*433-23_*433-21delins...
ENST00000350303.9:c.412-23_412-21delinsCCA ENSP00000344152.5:n.412-23_412-21delinsCC...
ENST00000356839.9:c.478-23_478-21delinsCCA ENSP00000349297.5:n.478-23_478-21delinsCC...
ENST00000543245.6:c.547-23_547-21delinsCCA ENSP00000438689.2:n.547-23_547-21delinsCC...
ENST00000577191.5:n.555-23_555-21delinsCCA
ENST00000577433.5:n.686-23_686-21delinsCCA
ENST00000577857.5:n.294-23_294-21delinsCCA
ENST00000579286.5:n.659-23_659-21delinsCCA
ENST00000579886.2:c.316-23_316-21delinsCCA ENSP00000463246.1:n.316-23_316-21delinsCC...
ENST00000580365.1:n.209-23_209-21delinsCCA
ENST00000581378.5:c.177-4_177-2delinsCCA
ENST00000581562.5:n.525-437_525-435delinsCCA
ENST00000582166.1:n.459-23_459-21delinsCCA
ENST00000583312.5:c.478-23_478-21delinsCCA ENSP00000467920.1:n.478-23_478-21delinsCC...
ENST00000583760.1:n.237_239delinsCCA
NM_000018.3:c.478-23_478-21delinsCCA NP_000009.1:n.478-23_478-21delinsCCA
NM_001033859.2:c.412-23_412-21delinsCCA NP_001029031.1:n.412-23_412-21delinsCCA
NM_001270447.1:c.547-23_547-21delinsCCA NP_001257376.1:n.547-23_547-21delinsCCA
NM_001270448.1:c.250-23_250-21delinsCCA NP_001257377.1:n.250-23_250-21delinsCCA
XM_006721516.2:c.478-23_478-21delinsCCA XP_006721579.2:n.478-23_478-21delinsCCA
XM_011523829.1:c.478-23_478-21delinsCCA XP_011522131.1:n.478-23_478-21delinsCCA
XM_011523830.1:c.478-23_478-21delinsCCA XP_011522132.1:n.478-23_478-21delinsCCA
XR_934021.1:n.585-23_585-21delinsCCA
XR_934022.1:n.585-23_585-21delinsCCA
XR_934023.1:n.585-23_585-21delinsCCA
XM_006721516.3:c.478-23_478-21delinsCCA XP_006721579.2:n.478-23_478-21delinsCCA
XM_011523829.2:c.478-23_478-21delinsCCA XP_011522131.1:n.478-23_478-21delinsCCA
XM_011523830.2:c.478-23_478-21delinsCCA XP_011522132.1:n.478-23_478-21delinsCCA
XM_024450741.1:c.478-23_478-21delinsCCA XP_024306509.1:n.478-23_478-21delinsCCA
XR_934021.2:n.537-23_537-21delinsCCA
XR_934022.2:n.537-23_537-21delinsCCA
XR_934023.2:n.537-23_537-21delinsCCA
NM_000018.4:c.478-23_478-21delinsCCA MANE Select NP_000009.1:n.478-23_478-21delinsCCA
NM_001033859.3:c.412-23_412-21delinsCCA NP_001029031.1:n.412-23_412-21delinsCCA
NM_001270447.2:c.547-23_547-21delinsCCA NP_001257376.1:n.547-23_547-21delinsCCA
NM_001270448.2:c.250-23_250-21delinsCCA NP_001257377.1:n.250-23_250-21delinsCCA