Canonical Allele Identifier: CA287435840
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs550244891

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221301_7221302del , CM000679.2:g.7221301_7221302del GRCh38
NC_000017.10:g.7124620_7124621del , CM000679.1:g.7124620_7124621del GRCh37
NC_000017.9:g.7065344_7065345del NCBI36
NG_007975.1:g.6468_6469del
NG_008391.2:g.3749_3750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-237_478-236del MANE Select ENSP00000349297.5:n.478-237_478-236del
ENST00000322910.9:c.*433-237_*433-236del ENSP00000325395.5:n.*433-237_*433-236del
ENST00000350303.9:c.412-237_412-236del ENSP00000344152.5:n.412-237_412-236del
ENST00000356839.9:c.478-237_478-236del ENSP00000349297.5:n.478-237_478-236del
ENST00000543245.6:c.547-237_547-236del ENSP00000438689.2:n.547-237_547-236del
ENST00000577191.5:n.555-237_555-236del
ENST00000577433.5:n.686-237_686-236del
ENST00000577857.5:n.294-237_294-236del
ENST00000579286.5:n.659-237_659-236del
ENST00000579886.2:c.316-237_316-236del ENSP00000463246.1:n.316-237_316-236del
ENST00000580365.1:n.209-237_209-236del
ENST00000581378.5:c.177-218_177-217del
ENST00000581562.5:n.524+243_524+244del
ENST00000582166.1:n.459-237_459-236del
ENST00000583312.5:c.478-237_478-236del ENSP00000467920.1:n.478-237_478-236del
ENST00000583760.1:n.23_24del
NM_000018.3:c.478-237_478-236del NP_000009.1:n.478-237_478-236del
NM_001033859.2:c.412-237_412-236del NP_001029031.1:n.412-237_412-236del
NM_001270447.1:c.547-237_547-236del NP_001257376.1:n.547-237_547-236del
NM_001270448.1:c.250-237_250-236del NP_001257377.1:n.250-237_250-236del
XM_006721516.2:c.478-237_478-236del XP_006721579.2:n.478-237_478-236del
XM_011523829.1:c.478-237_478-236del XP_011522131.1:n.478-237_478-236del
XM_011523830.1:c.478-237_478-236del XP_011522132.1:n.478-237_478-236del
XR_934021.1:n.585-237_585-236del
XR_934022.1:n.585-237_585-236del
XR_934023.1:n.585-237_585-236del
XM_006721516.3:c.478-237_478-236del XP_006721579.2:n.478-237_478-236del
XM_011523829.2:c.478-237_478-236del XP_011522131.1:n.478-237_478-236del
XM_011523830.2:c.478-237_478-236del XP_011522132.1:n.478-237_478-236del
XM_024450741.1:c.478-237_478-236del XP_024306509.1:n.478-237_478-236del
XR_934021.2:n.537-237_537-236del
XR_934022.2:n.537-237_537-236del
XR_934023.2:n.537-237_537-236del
NM_000018.4:c.478-237_478-236del MANE Select NP_000009.1:n.478-237_478-236del
NM_001033859.3:c.412-237_412-236del NP_001029031.1:n.412-237_412-236del
NM_001270447.2:c.547-237_547-236del NP_001257376.1:n.547-237_547-236del
NM_001270448.2:c.250-237_250-236del NP_001257377.1:n.250-237_250-236del