Canonical Allele Identifier: CA2245699793
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221431_7221432delinsGT , CM000679.2:g.7221431_7221432delinsGT GRCh38
NC_000017.10:g.7124750_7124751delinsGT , CM000679.1:g.7124750_7124751delinsGT GRCh37
NC_000017.9:g.7065474_7065475delinsGT NCBI36
NG_007975.1:g.6598_6599delinsGT
NG_008391.2:g.3619_3620delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-107_478-106delinsGT MANE Select ENSP00000349297.5:n.478-107_478-106delinsGT
ENST00000322910.9:c.*433-107_*433-106delinsGT ENSP00000325395.5:n.*433-107_*433-106delinsGT
ENST00000350303.9:c.412-107_412-106delinsGT ENSP00000344152.5:n.412-107_412-106delinsGT
ENST00000356839.9:c.478-107_478-106delinsGT ENSP00000349297.5:n.478-107_478-106delinsGT
ENST00000543245.6:c.547-107_547-106delinsGT ENSP00000438689.2:n.547-107_547-106delinsGT
ENST00000577191.5:n.555-107_555-106delinsGT
ENST00000577433.5:n.686-107_686-106delinsGT
ENST00000577857.5:n.294-107_294-106delinsGT
ENST00000579286.5:n.659-107_659-106delinsGT
ENST00000579886.2:c.316-107_316-106delinsGT ENSP00000463246.1:n.316-107_316-106delinsGT
ENST00000580365.1:n.209-107_209-106delinsGT
ENST00000581378.5:c.177-88_177-87delinsGT
ENST00000581562.5:n.524+373_524+374delinsGT
ENST00000582166.1:n.459-107_459-106delinsGT
ENST00000583312.5:c.478-107_478-106delinsGT ENSP00000467920.1:n.478-107_478-106delinsGT
ENST00000583760.1:n.153_154delinsGT
NM_000018.3:c.478-107_478-106delinsGT NP_000009.1:n.478-107_478-106delinsGT
NM_001033859.2:c.412-107_412-106delinsGT NP_001029031.1:n.412-107_412-106delinsGT
NM_001270447.1:c.547-107_547-106delinsGT NP_001257376.1:n.547-107_547-106delinsGT
NM_001270448.1:c.250-107_250-106delinsGT NP_001257377.1:n.250-107_250-106delinsGT
XM_006721516.2:c.478-107_478-106delinsGT XP_006721579.2:n.478-107_478-106delinsGT
XM_011523829.1:c.478-107_478-106delinsGT XP_011522131.1:n.478-107_478-106delinsGT
XM_011523830.1:c.478-107_478-106delinsGT XP_011522132.1:n.478-107_478-106delinsGT
XR_934021.1:n.585-107_585-106delinsGT
XR_934022.1:n.585-107_585-106delinsGT
XR_934023.1:n.585-107_585-106delinsGT
XM_006721516.3:c.478-107_478-106delinsGT XP_006721579.2:n.478-107_478-106delinsGT
XM_011523829.2:c.478-107_478-106delinsGT XP_011522131.1:n.478-107_478-106delinsGT
XM_011523830.2:c.478-107_478-106delinsGT XP_011522132.1:n.478-107_478-106delinsGT
XM_024450741.1:c.478-107_478-106delinsGT XP_024306509.1:n.478-107_478-106delinsGT
XR_934021.2:n.537-107_537-106delinsGT
XR_934022.2:n.537-107_537-106delinsGT
XR_934023.2:n.537-107_537-106delinsGT
NM_000018.4:c.478-107_478-106delinsGT MANE Select NP_000009.1:n.478-107_478-106delinsGT
NM_001033859.3:c.412-107_412-106delinsGT NP_001029031.1:n.412-107_412-106delinsGT
NM_001270447.2:c.547-107_547-106delinsGT NP_001257376.1:n.547-107_547-106delinsGT
NM_001270448.2:c.250-107_250-106delinsGT NP_001257377.1:n.250-107_250-106delinsGT