Canonical Allele Identifier: CA2635781148
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221446_7221447del , CM000679.2:g.7221446_7221447del GRCh38
NC_000017.10:g.7124765_7124766del , CM000679.1:g.7124765_7124766del GRCh37
NC_000017.9:g.7065489_7065490del NCBI36
NG_007975.1:g.6613_6614del
NG_008391.2:g.3604_3605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-92_478-91del MANE Select ENSP00000349297.5:n.478-92_478-91del
ENST00000322910.9:c.*433-92_*433-91del ENSP00000325395.5:n.*433-92_*433-91del
ENST00000350303.9:c.412-92_412-91del ENSP00000344152.5:n.412-92_412-91del
ENST00000356839.9:c.478-92_478-91del ENSP00000349297.5:n.478-92_478-91del
ENST00000543245.6:c.547-92_547-91del ENSP00000438689.2:n.547-92_547-91del
ENST00000577191.5:n.555-92_555-91del
ENST00000577433.5:n.686-92_686-91del
ENST00000577857.5:n.294-92_294-91del
ENST00000579286.5:n.659-92_659-91del
ENST00000579886.2:c.316-92_316-91del ENSP00000463246.1:n.316-92_316-91del
ENST00000580365.1:n.209-92_209-91del
ENST00000581378.5:c.177-73_177-72del
ENST00000581562.5:n.524+388_524+389del
ENST00000582166.1:n.459-92_459-91del
ENST00000583312.5:c.478-92_478-91del ENSP00000467920.1:n.478-92_478-91del
ENST00000583760.1:n.168_169del
NM_000018.3:c.478-92_478-91del NP_000009.1:n.478-92_478-91del
NM_001033859.2:c.412-92_412-91del NP_001029031.1:n.412-92_412-91del
NM_001270447.1:c.547-92_547-91del NP_001257376.1:n.547-92_547-91del
NM_001270448.1:c.250-92_250-91del NP_001257377.1:n.250-92_250-91del
XM_006721516.2:c.478-92_478-91del XP_006721579.2:n.478-92_478-91del
XM_011523829.1:c.478-92_478-91del XP_011522131.1:n.478-92_478-91del
XM_011523830.1:c.478-92_478-91del XP_011522132.1:n.478-92_478-91del
XR_934021.1:n.585-92_585-91del
XR_934022.1:n.585-92_585-91del
XR_934023.1:n.585-92_585-91del
XM_006721516.3:c.478-92_478-91del XP_006721579.2:n.478-92_478-91del
XM_011523829.2:c.478-92_478-91del XP_011522131.1:n.478-92_478-91del
XM_011523830.2:c.478-92_478-91del XP_011522132.1:n.478-92_478-91del
XM_024450741.1:c.478-92_478-91del XP_024306509.1:n.478-92_478-91del
XR_934021.2:n.537-92_537-91del
XR_934022.2:n.537-92_537-91del
XR_934023.2:n.537-92_537-91del
NM_000018.4:c.478-92_478-91del MANE Select NP_000009.1:n.478-92_478-91del
NM_001033859.3:c.412-92_412-91del NP_001029031.1:n.412-92_412-91del
NM_001270447.2:c.547-92_547-91del NP_001257376.1:n.547-92_547-91del
NM_001270448.2:c.250-92_250-91del NP_001257377.1:n.250-92_250-91del