Canonical Allele Identifier: CA2635781055
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221423_7221437del , CM000679.2:g.7221423_7221437del GRCh38
NC_000017.10:g.7124742_7124756del , CM000679.1:g.7124742_7124756del GRCh37
NC_000017.9:g.7065466_7065480del NCBI36
NG_007975.1:g.6590_6604del
NG_008391.2:g.3614_3628del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-115_478-101del MANE Select ENSP00000349297.5:n.478-115_478-101del
ENST00000322910.9:c.*433-115_*433-101del ENSP00000325395.5:n.*433-115_*433-101del
ENST00000350303.9:c.412-115_412-101del ENSP00000344152.5:n.412-115_412-101del
ENST00000356839.9:c.478-115_478-101del ENSP00000349297.5:n.478-115_478-101del
ENST00000543245.6:c.547-115_547-101del ENSP00000438689.2:n.547-115_547-101del
ENST00000577191.5:n.555-115_555-101del
ENST00000577433.5:n.686-115_686-101del
ENST00000577857.5:n.294-115_294-101del
ENST00000579286.5:n.659-115_659-101del
ENST00000579886.2:c.316-115_316-101del ENSP00000463246.1:n.316-115_316-101del
ENST00000580365.1:n.209-115_209-101del
ENST00000581378.5:c.177-96_177-82del
ENST00000581562.5:n.524+365_524+379del
ENST00000582166.1:n.459-115_459-101del
ENST00000583312.5:c.478-115_478-101del ENSP00000467920.1:n.478-115_478-101del
ENST00000583760.1:n.145_159del
NM_000018.3:c.478-115_478-101del NP_000009.1:n.478-115_478-101del
NM_001033859.2:c.412-115_412-101del NP_001029031.1:n.412-115_412-101del
NM_001270447.1:c.547-115_547-101del NP_001257376.1:n.547-115_547-101del
NM_001270448.1:c.250-115_250-101del NP_001257377.1:n.250-115_250-101del
XM_006721516.2:c.478-115_478-101del XP_006721579.2:n.478-115_478-101del
XM_011523829.1:c.478-115_478-101del XP_011522131.1:n.478-115_478-101del
XM_011523830.1:c.478-115_478-101del XP_011522132.1:n.478-115_478-101del
XR_934021.1:n.585-115_585-101del
XR_934022.1:n.585-115_585-101del
XR_934023.1:n.585-115_585-101del
XM_006721516.3:c.478-115_478-101del XP_006721579.2:n.478-115_478-101del
XM_011523829.2:c.478-115_478-101del XP_011522131.1:n.478-115_478-101del
XM_011523830.2:c.478-115_478-101del XP_011522132.1:n.478-115_478-101del
XM_024450741.1:c.478-115_478-101del XP_024306509.1:n.478-115_478-101del
XR_934021.2:n.537-115_537-101del
XR_934022.2:n.537-115_537-101del
XR_934023.2:n.537-115_537-101del
NM_000018.4:c.478-115_478-101del MANE Select NP_000009.1:n.478-115_478-101del
NM_001033859.3:c.412-115_412-101del NP_001029031.1:n.412-115_412-101del
NM_001270447.2:c.547-115_547-101del NP_001257376.1:n.547-115_547-101del
NM_001270448.2:c.250-115_250-101del NP_001257377.1:n.250-115_250-101del