Canonical Allele Identifier: CA2245699718
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221383_7221386delinsACTT , CM000679.2:g.7221383_7221386delinsACTT GRCh38
NC_000017.10:g.7124702_7124705delinsACTT , CM000679.1:g.7124702_7124705delinsACTT GRCh37
NC_000017.9:g.7065426_7065429delinsACTT NCBI36
NG_007975.1:g.6550_6553delinsACTT
NG_008391.2:g.3665_3668delinsAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-155_478-152delinsACTT MANE Select ENSP00000349297.5:n.478-155_478-152delinsACTT
ENST00000322910.9:c.*433-155_*433-152delinsACTT ENSP00000325395.5:n.*433-155_*433-152delinsACTT
ENST00000350303.9:c.412-155_412-152delinsACTT ENSP00000344152.5:n.412-155_412-152delinsACTT
ENST00000356839.9:c.478-155_478-152delinsACTT ENSP00000349297.5:n.478-155_478-152delinsACTT
ENST00000543245.6:c.547-155_547-152delinsACTT ENSP00000438689.2:n.547-155_547-152delinsACTT
ENST00000577191.5:n.555-155_555-152delinsACTT
ENST00000577433.5:n.686-155_686-152delinsACTT
ENST00000577857.5:n.294-155_294-152delinsACTT
ENST00000579286.5:n.659-155_659-152delinsACTT
ENST00000579886.2:c.316-155_316-152delinsACTT ENSP00000463246.1:n.316-155_316-152delinsACTT
ENST00000580365.1:n.209-155_209-152delinsACTT
ENST00000581378.5:c.177-136_177-133delinsACTT
ENST00000581562.5:n.524+325_524+328delinsACTT
ENST00000582166.1:n.459-155_459-152delinsACTT
ENST00000583312.5:c.478-155_478-152delinsACTT ENSP00000467920.1:n.478-155_478-152delinsACTT
ENST00000583760.1:n.105_108delinsACTT
NM_000018.3:c.478-155_478-152delinsACTT NP_000009.1:n.478-155_478-152delinsACTT
NM_001033859.2:c.412-155_412-152delinsACTT NP_001029031.1:n.412-155_412-152delinsACTT
NM_001270447.1:c.547-155_547-152delinsACTT NP_001257376.1:n.547-155_547-152delinsACTT
NM_001270448.1:c.250-155_250-152delinsACTT NP_001257377.1:n.250-155_250-152delinsACTT
XM_006721516.2:c.478-155_478-152delinsACTT XP_006721579.2:n.478-155_478-152delinsACTT
XM_011523829.1:c.478-155_478-152delinsACTT XP_011522131.1:n.478-155_478-152delinsACTT
XM_011523830.1:c.478-155_478-152delinsACTT XP_011522132.1:n.478-155_478-152delinsACTT
XR_934021.1:n.585-155_585-152delinsACTT
XR_934022.1:n.585-155_585-152delinsACTT
XR_934023.1:n.585-155_585-152delinsACTT
XM_006721516.3:c.478-155_478-152delinsACTT XP_006721579.2:n.478-155_478-152delinsACTT
XM_011523829.2:c.478-155_478-152delinsACTT XP_011522131.1:n.478-155_478-152delinsACTT
XM_011523830.2:c.478-155_478-152delinsACTT XP_011522132.1:n.478-155_478-152delinsACTT
XM_024450741.1:c.478-155_478-152delinsACTT XP_024306509.1:n.478-155_478-152delinsACTT
XR_934021.2:n.537-155_537-152delinsACTT
XR_934022.2:n.537-155_537-152delinsACTT
XR_934023.2:n.537-155_537-152delinsACTT
NM_000018.4:c.478-155_478-152delinsACTT MANE Select NP_000009.1:n.478-155_478-152delinsACTT
NM_001033859.3:c.412-155_412-152delinsACTT NP_001029031.1:n.412-155_412-152delinsACTT
NM_001270447.2:c.547-155_547-152delinsACTT NP_001257376.1:n.547-155_547-152delinsACTT
NM_001270448.2:c.250-155_250-152delinsACTT NP_001257377.1:n.250-155_250-152delinsACTT