Canonical Allele Identifier: CA2245697351

Gene: ACADVL DLG4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7219997_7220014delinsCGGATGGCCGCGAGCTTG , CM000679.2:g.7219997_7220014delinsCGGATGGCCGCGAGCTTG	GRCh38
NC_000017.10:g.7123316_7123333delinsCGGATGGCCGCGAGCTTG , CM000679.1:g.7123316_7123333delinsCGGATGGCCGCGAGCTTG	GRCh37
NC_000017.9:g.7064040_7064057delinsCGGATGGCCGCGAGCTTG	NCBI36
NG_007975.1:g.5164_5181delinsCGGATGGCCGCGAGCTTG
NG_008391.2:g.5037_5054delinsCAAGCTCGCGGCCATCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL) MANE Select	ENSP00000349297.5:p.Arg5=
ENST00000322910.9:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000325395.5:p.Arg5=
ENST00000350303.9:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000344152.5:p.Arg5=
ENST00000356839.9:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000349297.5:p.Arg5=
ENST00000543245.6:c.132-125_132-108delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000438689.2:n.132-125_132-108delinsCGGATGGCCGCGAGCTTG
ENST00000577191.5:n.90_107delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000577857.5:n.103_120delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000578269.5:n.120_137delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000578421.1:n.72_89delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000579286.5:n.120_137delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000579886.2:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000463246.1:p.Arg5=
ENST00000580263.5:n.103_120delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000581562.5:n.60_77delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000582056.5:n.103_120delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000582356.5:n.138_155delinsCGGATGGCCGCGAGCTTG (ACADVL)
ENST00000583312.5:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000467920.1:p.Arg5=
ENST00000584103.5:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	ENSP00000465353.1:p.Arg5=
NM_000018.3:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_000009.1:p.Arg5=
NM_001033859.2:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_001029031.1:p.Arg5=
NM_001270447.1:c.132-125_132-108delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_001257376.1:n.132-125_132-108delinsCGGATGGCCGCGAGCTTG
NM_001270448.1:c.-291_-274delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_001257377.1:n.-291_-274delinsCGGATGGCCGCGAGCTTG
NM_001365.3:c.-1165_-1148delinsCAAGCTCGCGGCCATCCG (DLG4)	NP_001356.1:n.-1165_-1148delinsCAAGCTCGCGGCCATCCG
XM_006721516.2:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_006721579.2:p.Arg5=
XM_011523829.1:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_011522131.1:p.Arg5=
XM_011523830.1:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_011522132.1:p.Arg5=
XR_934021.1:n.120_137delinsCGGATGGCCGCGAGCTTG (ACADVL)
XR_934022.1:n.120_137delinsCGGATGGCCGCGAGCTTG (ACADVL)
XR_934023.1:n.120_137delinsCGGATGGCCGCGAGCTTG (ACADVL)
NM_001321074.1:c.-1165_-1148delinsCAAGCTCGCGGCCATCCG (DLG4)	NP_001308003.1:n.-1165_-1148delinsCAAGCTCGCGGCCATCCG
NM_001365.4:c.-1165_-1148delinsCAAGCTCGCGGCCATCCG (DLG4)	NP_001356.1:n.-1165_-1148delinsCAAGCTCGCGGCCATCCG
NR_135527.1:n.37_54delinsCAAGCTCGCGGCCATCCG (DLG4)
XM_006721516.3:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_006721579.2:p.Arg5=
XM_011523829.2:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_011522131.1:p.Arg5=
XM_011523830.2:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_011522132.1:p.Arg5=
XM_024450741.1:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	XP_024306509.1:p.Arg5=
XR_934021.2:n.72_89delinsCGGATGGCCGCGAGCTTG (ACADVL)
XR_934022.2:n.72_89delinsCGGATGGCCGCGAGCTTG (ACADVL)
XR_934023.2:n.72_89delinsCGGATGGCCGCGAGCTTG (ACADVL)
NM_000018.4:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL) MANE Select	NP_000009.1:p.Arg5=
NM_001033859.3:c.13_30delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_001029031.1:p.Arg5=
NM_001270447.2:c.132-125_132-108delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_001257376.1:n.132-125_132-108delinsCGGATGGCCGCGAGCTTG
NM_001270448.2:c.-291_-274delinsCGGATGGCCGCGAGCTTG (ACADVL)	NP_001257377.1:n.-291_-274delinsCGGATGGCCGCGAGCTTG