Canonical Allele Identifier: CA981152593
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071213003

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221423_7221424del , CM000679.2:g.7221423_7221424del GRCh38
NC_000017.10:g.7124742_7124743del , CM000679.1:g.7124742_7124743del GRCh37
NC_000017.9:g.7065466_7065467del NCBI36
NG_007975.1:g.6590_6591del
NG_008391.2:g.3627_3628del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-115_478-114del MANE Select ENSP00000349297.5:n.478-115_478-114del
ENST00000322910.9:c.*433-115_*433-114del ENSP00000325395.5:n.*433-115_*433-114del
ENST00000350303.9:c.412-115_412-114del ENSP00000344152.5:n.412-115_412-114del
ENST00000356839.9:c.478-115_478-114del ENSP00000349297.5:n.478-115_478-114del
ENST00000543245.6:c.547-115_547-114del ENSP00000438689.2:n.547-115_547-114del
ENST00000577191.5:n.555-115_555-114del
ENST00000577433.5:n.686-115_686-114del
ENST00000577857.5:n.294-115_294-114del
ENST00000579286.5:n.659-115_659-114del
ENST00000579886.2:c.316-115_316-114del ENSP00000463246.1:n.316-115_316-114del
ENST00000580365.1:n.209-115_209-114del
ENST00000581378.5:c.177-96_177-95del
ENST00000581562.5:n.524+365_524+366del
ENST00000582166.1:n.459-115_459-114del
ENST00000583312.5:c.478-115_478-114del ENSP00000467920.1:n.478-115_478-114del
ENST00000583760.1:n.145_146del
NM_000018.3:c.478-115_478-114del NP_000009.1:n.478-115_478-114del
NM_001033859.2:c.412-115_412-114del NP_001029031.1:n.412-115_412-114del
NM_001270447.1:c.547-115_547-114del NP_001257376.1:n.547-115_547-114del
NM_001270448.1:c.250-115_250-114del NP_001257377.1:n.250-115_250-114del
XM_006721516.2:c.478-115_478-114del XP_006721579.2:n.478-115_478-114del
XM_011523829.1:c.478-115_478-114del XP_011522131.1:n.478-115_478-114del
XM_011523830.1:c.478-115_478-114del XP_011522132.1:n.478-115_478-114del
XR_934021.1:n.585-115_585-114del
XR_934022.1:n.585-115_585-114del
XR_934023.1:n.585-115_585-114del
XM_006721516.3:c.478-115_478-114del XP_006721579.2:n.478-115_478-114del
XM_011523829.2:c.478-115_478-114del XP_011522131.1:n.478-115_478-114del
XM_011523830.2:c.478-115_478-114del XP_011522132.1:n.478-115_478-114del
XM_024450741.1:c.478-115_478-114del XP_024306509.1:n.478-115_478-114del
XR_934021.2:n.537-115_537-114del
XR_934022.2:n.537-115_537-114del
XR_934023.2:n.537-115_537-114del
NM_000018.4:c.478-115_478-114del MANE Select NP_000009.1:n.478-115_478-114del
NM_001033859.3:c.412-115_412-114del NP_001029031.1:n.412-115_412-114del
NM_001270447.2:c.547-115_547-114del NP_001257376.1:n.547-115_547-114del
NM_001270448.2:c.250-115_250-114del NP_001257377.1:n.250-115_250-114del