Canonical Allele Identifier: CA287435966
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs535609436

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221420_7221436del , CM000679.2:g.7221420_7221436del GRCh38
NC_000017.10:g.7124739_7124755del , CM000679.1:g.7124739_7124755del GRCh37
NC_000017.9:g.7065463_7065479del NCBI36
NG_007975.1:g.6587_6603del
NG_008391.2:g.3623_3639del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-118_478-102del MANE Select ENSP00000349297.5:n.478-118_478-102del
ENST00000322910.9:c.*433-118_*433-102del ENSP00000325395.5:n.*433-118_*433-102del
ENST00000350303.9:c.412-118_412-102del ENSP00000344152.5:n.412-118_412-102del
ENST00000356839.9:c.478-118_478-102del ENSP00000349297.5:n.478-118_478-102del
ENST00000543245.6:c.547-118_547-102del ENSP00000438689.2:n.547-118_547-102del
ENST00000577191.5:n.555-118_555-102del
ENST00000577433.5:n.686-118_686-102del
ENST00000577857.5:n.294-118_294-102del
ENST00000579286.5:n.659-118_659-102del
ENST00000579886.2:c.316-118_316-102del ENSP00000463246.1:n.316-118_316-102del
ENST00000580365.1:n.209-118_209-102del
ENST00000581378.5:c.177-99_177-83del
ENST00000581562.5:n.524+362_524+378del
ENST00000582166.1:n.459-118_459-102del
ENST00000583312.5:c.478-118_478-102del ENSP00000467920.1:n.478-118_478-102del
ENST00000583760.1:n.142_158del
NM_000018.3:c.478-118_478-102del NP_000009.1:n.478-118_478-102del
NM_001033859.2:c.412-118_412-102del NP_001029031.1:n.412-118_412-102del
NM_001270447.1:c.547-118_547-102del NP_001257376.1:n.547-118_547-102del
NM_001270448.1:c.250-118_250-102del NP_001257377.1:n.250-118_250-102del
XM_006721516.2:c.478-118_478-102del XP_006721579.2:n.478-118_478-102del
XM_011523829.1:c.478-118_478-102del XP_011522131.1:n.478-118_478-102del
XM_011523830.1:c.478-118_478-102del XP_011522132.1:n.478-118_478-102del
XR_934021.1:n.585-118_585-102del
XR_934022.1:n.585-118_585-102del
XR_934023.1:n.585-118_585-102del
XM_006721516.3:c.478-118_478-102del XP_006721579.2:n.478-118_478-102del
XM_011523829.2:c.478-118_478-102del XP_011522131.1:n.478-118_478-102del
XM_011523830.2:c.478-118_478-102del XP_011522132.1:n.478-118_478-102del
XM_024450741.1:c.478-118_478-102del XP_024306509.1:n.478-118_478-102del
XR_934021.2:n.537-118_537-102del
XR_934022.2:n.537-118_537-102del
XR_934023.2:n.537-118_537-102del
NM_000018.4:c.478-118_478-102del MANE Select NP_000009.1:n.478-118_478-102del
NM_001033859.3:c.412-118_412-102del NP_001029031.1:n.412-118_412-102del
NM_001270447.2:c.547-118_547-102del NP_001257376.1:n.547-118_547-102del
NM_001270448.2:c.250-118_250-102del NP_001257377.1:n.250-118_250-102del