Canonical Allele Identifier: CA913013618

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219997_7220014del , CM000679.2:g.7219997_7220014del GRCh38
NC_000017.10:g.7123316_7123333del , CM000679.1:g.7123316_7123333del GRCh37
NC_000017.9:g.7064040_7064057del NCBI36
NG_007975.1:g.5164_5181del
NG_008391.2:g.5037_5054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.13_30del (ACADVL) MANE Select ENSP00000349297.5:p.Arg5_Leu10del
ENST00000322910.9:c.13_30del (ACADVL) ENSP00000325395.5:p.Arg5_Leu10del
ENST00000350303.9:c.13_30del (ACADVL) ENSP00000344152.5:p.Arg5_Leu10del
ENST00000356839.9:c.13_30del (ACADVL) ENSP00000349297.5:p.Arg5_Leu10del
ENST00000543245.6:c.132-125_132-108del (ACADVL) ENSP00000438689.2:n.132-125_132-108del
ENST00000577191.5:n.90_107del (ACADVL)
ENST00000577857.5:n.103_120del (ACADVL)
ENST00000578269.5:n.120_137del (ACADVL)
ENST00000578421.1:n.72_89del (ACADVL)
ENST00000579286.5:n.120_137del (ACADVL)
ENST00000579886.2:c.13_30del (ACADVL) ENSP00000463246.1:p.Arg5_Leu10del
ENST00000580263.5:n.103_120del (ACADVL)
ENST00000581562.5:n.60_77del (ACADVL)
ENST00000582056.5:n.103_120del (ACADVL)
ENST00000582356.5:n.138_155del (ACADVL)
ENST00000583312.5:c.13_30del (ACADVL) ENSP00000467920.1:p.Arg5_Leu10del
ENST00000584103.5:c.13_30del (ACADVL) ENSP00000465353.1:p.Arg5_Leu10del
NM_000018.3:c.13_30del (ACADVL) NP_000009.1:p.Arg5_Leu10del
NM_001033859.2:c.13_30del (ACADVL) NP_001029031.1:p.Arg5_Leu10del
NM_001270447.1:c.132-125_132-108del (ACADVL) NP_001257376.1:n.132-125_132-108del
NM_001270448.1:c.-291_-274del (ACADVL) NP_001257377.1:n.-291_-274del
NM_001365.3:c.-1165_-1148del (DLG4) NP_001356.1:n.-1165_-1148del
XM_006721516.2:c.13_30del (ACADVL) XP_006721579.2:p.Arg5_Leu10del
XM_011523829.1:c.13_30del (ACADVL) XP_011522131.1:p.Arg5_Leu10del
XM_011523830.1:c.13_30del (ACADVL) XP_011522132.1:p.Arg5_Leu10del
XR_934021.1:n.120_137del (ACADVL)
XR_934022.1:n.120_137del (ACADVL)
XR_934023.1:n.120_137del (ACADVL)
NM_001321074.1:c.-1165_-1148del (DLG4) NP_001308003.1:n.-1165_-1148del
NM_001365.4:c.-1165_-1148del (DLG4) NP_001356.1:n.-1165_-1148del
NR_135527.1:n.37_54del (DLG4)
XM_006721516.3:c.13_30del (ACADVL) XP_006721579.2:p.Arg5_Leu10del
XM_011523829.2:c.13_30del (ACADVL) XP_011522131.1:p.Arg5_Leu10del
XM_011523830.2:c.13_30del (ACADVL) XP_011522132.1:p.Arg5_Leu10del
XM_024450741.1:c.13_30del (ACADVL) XP_024306509.1:p.Arg5_Leu10del
XR_934021.2:n.72_89del (ACADVL)
XR_934022.2:n.72_89del (ACADVL)
XR_934023.2:n.72_89del (ACADVL)
NM_000018.4:c.13_30del (ACADVL) MANE Select NP_000009.1:p.Arg5_Leu10del
NM_001033859.3:c.13_30del (ACADVL) NP_001029031.1:p.Arg5_Leu10del
NM_001270447.2:c.132-125_132-108del (ACADVL) NP_001257376.1:n.132-125_132-108del
NM_001270448.2:c.-291_-274del (ACADVL) NP_001257377.1:n.-291_-274del