Canonical Allele Identifier: CA2245700698
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221890_7221891delinsGT , CM000679.2:g.7221890_7221891delinsGT GRCh38
NC_000017.10:g.7125209_7125210delinsGT , CM000679.1:g.7125209_7125210delinsGT GRCh37
NC_000017.9:g.7065933_7065934delinsGT NCBI36
NG_007975.1:g.7057_7058delinsGT
NG_008391.2:g.3160_3161delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.623-62_623-61delinsGT MANE Select ENSP00000349297.5:n.623-62_623-61delinsGT
ENST00000322910.9:c.*578-62_*578-61delinsGT ENSP00000325395.5:n.*578-62_*578-61delinsGT
ENST00000350303.9:c.557-62_557-61delinsGT ENSP00000344152.5:n.557-62_557-61delinsGT
ENST00000356839.9:c.623-62_623-61delinsGT ENSP00000349297.5:n.623-62_623-61delinsGT
ENST00000543245.6:c.692-62_692-61delinsGT ENSP00000438689.2:n.692-62_692-61delinsGT
ENST00000577191.5:n.700-62_700-61delinsGT
ENST00000577857.5:n.439-62_439-61delinsGT
ENST00000579286.5:n.804-62_804-61delinsGT
ENST00000579886.2:c.461-62_461-61delinsGT ENSP00000463246.1:n.461-62_461-61delinsGT
ENST00000580365.1:n.354-62_354-61delinsGT
ENST00000581378.5:c.341-62_341-61delinsGT
ENST00000581562.5:n.525-62_525-61delinsGT
ENST00000583312.5:c.623-47_623-46delinsGT ENSP00000467920.1:n.623-47_623-46delinsGT
ENST00000583760.1:n.405-62_405-61delinsGT
NM_000018.3:c.623-62_623-61delinsGT NP_000009.1:n.623-62_623-61delinsGT
NM_001033859.2:c.557-62_557-61delinsGT NP_001029031.1:n.557-62_557-61delinsGT
NM_001270447.1:c.692-62_692-61delinsGT NP_001257376.1:n.692-62_692-61delinsGT
NM_001270448.1:c.395-62_395-61delinsGT NP_001257377.1:n.395-62_395-61delinsGT
XM_006721516.2:c.623-62_623-61delinsGT XP_006721579.2:n.623-62_623-61delinsGT
XM_011523829.1:c.623-62_623-61delinsGT XP_011522131.1:n.623-62_623-61delinsGT
XM_011523830.1:c.623-62_623-61delinsGT XP_011522132.1:n.623-62_623-61delinsGT
XR_934021.1:n.730-62_730-61delinsGT
XR_934022.1:n.730-62_730-61delinsGT
XR_934023.1:n.730-62_730-61delinsGT
XM_006721516.3:c.623-62_623-61delinsGT XP_006721579.2:n.623-62_623-61delinsGT
XM_011523829.2:c.623-62_623-61delinsGT XP_011522131.1:n.623-62_623-61delinsGT
XM_011523830.2:c.623-62_623-61delinsGT XP_011522132.1:n.623-62_623-61delinsGT
XM_024450741.1:c.623-62_623-61delinsGT XP_024306509.1:n.623-62_623-61delinsGT
XR_934021.2:n.682-62_682-61delinsGT
XR_934022.2:n.682-62_682-61delinsGT
XR_934023.2:n.682-62_682-61delinsGT
NM_000018.4:c.623-62_623-61delinsGT MANE Select NP_000009.1:n.623-62_623-61delinsGT
NM_001033859.3:c.557-62_557-61delinsGT NP_001029031.1:n.557-62_557-61delinsGT
NM_001270447.2:c.692-62_692-61delinsGT NP_001257376.1:n.692-62_692-61delinsGT
NM_001270448.2:c.395-62_395-61delinsGT NP_001257377.1:n.395-62_395-61delinsGT