Canonical Allele Identifier: CA2245699713
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221380_7221383delinsCCCA , CM000679.2:g.7221380_7221383delinsCCCA GRCh38
NC_000017.10:g.7124699_7124702delinsCCCA , CM000679.1:g.7124699_7124702delinsCCCA GRCh37
NC_000017.9:g.7065423_7065426delinsCCCA NCBI36
NG_007975.1:g.6547_6550delinsCCCA
NG_008391.2:g.3668_3671delinsTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-158_478-155delinsCCCA MANE Select ENSP00000349297.5:n.478-158_478-155delinsCCCA
ENST00000322910.9:c.*433-158_*433-155delinsCCCA ENSP00000325395.5:n.*433-158_*433-155delinsCCCA
ENST00000350303.9:c.412-158_412-155delinsCCCA ENSP00000344152.5:n.412-158_412-155delinsCCCA
ENST00000356839.9:c.478-158_478-155delinsCCCA ENSP00000349297.5:n.478-158_478-155delinsCCCA
ENST00000543245.6:c.547-158_547-155delinsCCCA ENSP00000438689.2:n.547-158_547-155delinsCCCA
ENST00000577191.5:n.555-158_555-155delinsCCCA
ENST00000577433.5:n.686-158_686-155delinsCCCA
ENST00000577857.5:n.294-158_294-155delinsCCCA
ENST00000579286.5:n.659-158_659-155delinsCCCA
ENST00000579886.2:c.316-158_316-155delinsCCCA ENSP00000463246.1:n.316-158_316-155delinsCCCA
ENST00000580365.1:n.209-158_209-155delinsCCCA
ENST00000581378.5:c.177-139_177-136delinsCCCA
ENST00000581562.5:n.524+322_524+325delinsCCCA
ENST00000582166.1:n.459-158_459-155delinsCCCA
ENST00000583312.5:c.478-158_478-155delinsCCCA ENSP00000467920.1:n.478-158_478-155delinsCCCA
ENST00000583760.1:n.102_105delinsCCCA
NM_000018.3:c.478-158_478-155delinsCCCA NP_000009.1:n.478-158_478-155delinsCCCA
NM_001033859.2:c.412-158_412-155delinsCCCA NP_001029031.1:n.412-158_412-155delinsCCCA
NM_001270447.1:c.547-158_547-155delinsCCCA NP_001257376.1:n.547-158_547-155delinsCCCA
NM_001270448.1:c.250-158_250-155delinsCCCA NP_001257377.1:n.250-158_250-155delinsCCCA
XM_006721516.2:c.478-158_478-155delinsCCCA XP_006721579.2:n.478-158_478-155delinsCCCA
XM_011523829.1:c.478-158_478-155delinsCCCA XP_011522131.1:n.478-158_478-155delinsCCCA
XM_011523830.1:c.478-158_478-155delinsCCCA XP_011522132.1:n.478-158_478-155delinsCCCA
XR_934021.1:n.585-158_585-155delinsCCCA
XR_934022.1:n.585-158_585-155delinsCCCA
XR_934023.1:n.585-158_585-155delinsCCCA
XM_006721516.3:c.478-158_478-155delinsCCCA XP_006721579.2:n.478-158_478-155delinsCCCA
XM_011523829.2:c.478-158_478-155delinsCCCA XP_011522131.1:n.478-158_478-155delinsCCCA
XM_011523830.2:c.478-158_478-155delinsCCCA XP_011522132.1:n.478-158_478-155delinsCCCA
XM_024450741.1:c.478-158_478-155delinsCCCA XP_024306509.1:n.478-158_478-155delinsCCCA
XR_934021.2:n.537-158_537-155delinsCCCA
XR_934022.2:n.537-158_537-155delinsCCCA
XR_934023.2:n.537-158_537-155delinsCCCA
NM_000018.4:c.478-158_478-155delinsCCCA MANE Select NP_000009.1:n.478-158_478-155delinsCCCA
NM_001033859.3:c.412-158_412-155delinsCCCA NP_001029031.1:n.412-158_412-155delinsCCCA
NM_001270447.2:c.547-158_547-155delinsCCCA NP_001257376.1:n.547-158_547-155delinsCCCA
NM_001270448.2:c.250-158_250-155delinsCCCA NP_001257377.1:n.250-158_250-155delinsCCCA