Canonical Allele Identifier: CA915949498

Linked Data

ClinVar Variation Id: 555749
ClinVar RCV Id: RCV000671629
dbSNP Id: rs6145976

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219936_7219937insGGGCACGCGGGCGTGCAGGACGC , CM000679.2:g.7219936_7219937insGGGCACGCGGGCGTGCAGGACGC GRCh38
NC_000017.10:g.7123255_7123256insGGGCACGCGGGCGTGCAGGACGC , CM000679.1:g.7123255_7123256insGGGCACGCGGGCGTGCAGGACGC GRCh37
NC_000017.9:g.7063979_7063980insGGGCACGCGGGCGTGCAGGACGC NCBI36
NG_007975.1:g.5103_5104insGGGCACGCGGGCGTGCAGGACGC
NG_008391.2:g.5129_5130insGCGTGCCCGCGTCCTGCACGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) ENSP00000325395.5:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
ENST00000350303.9:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) ENSP00000344152.5:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
ENST00000356839.9:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) ENSP00000349297.5:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
ENST00000543245.6:c.132-186_132-185insGGGCACGCGGGCGTGCAGGACGC (ACADVL) ENSP00000438689.2:n.132-186_132-185insGGGCACGCGGGCGTGCAGGACGC...
ENST00000577191.5:n.29_30insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000577857.5:n.42_43insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000578269.5:n.59_60insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000579286.5:n.59_60insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000580263.5:n.42_43insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000582056.5:n.42_43insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000582356.5:n.77_78insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
ENST00000583312.5:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) ENSP00000467920.1:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
ENST00000584103.5:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) ENSP00000465353.1:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
NM_000018.3:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) NP_000009.1:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
NM_001033859.2:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) NP_001029031.1:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
NM_001270447.1:c.132-186_132-185insGGGCACGCGGGCGTGCAGGACGC (ACADVL) NP_001257376.1:n.132-186_132-185insGGGCACGCGGGCGTGCAGGACGC
NM_001270448.1:c.-352_-351insGGGCACGCGGGCGTGCAGGACGC (ACADVL) NP_001257377.1:n.-352_-351insGGGCACGCGGGCGTGCAGGACGC
NM_001365.3:c.-1073_-1072insGCGTGCCCGCGTCCTGCACGCCC (DLG4) NP_001356.1:n.-1073_-1072insGCGTGCCCGCGTCCTGCACGCCC
XM_006721516.2:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) XP_006721579.2:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
XM_011523829.1:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) XP_011522131.1:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
XM_011523830.1:c.-49_-48insGGGCACGCGGGCGTGCAGGACGC (ACADVL) XP_011522132.1:n.-49_-48insGGGCACGCGGGCGTGCAGGACGC
XR_934021.1:n.59_60insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
XR_934022.1:n.59_60insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
XR_934023.1:n.59_60insGGGCACGCGGGCGTGCAGGACGC (ACADVL)
NM_001321074.1:c.-1073_-1072insGCGTGCCCGCGTCCTGCACGCCC (DLG4) NP_001308003.1:n.-1073_-1072insGCGTGCCCGCGTCCTGCACGCCC
NM_001365.4:c.-1073_-1072insGCGTGCCCGCGTCCTGCACGCCC (DLG4) NP_001356.1:n.-1073_-1072insGCGTGCCCGCGTCCTGCACGCCC
NR_135527.1:n.129_130insGCGTGCCCGCGTCCTGCACGCCC (DLG4)
NM_001270447.2:c.132-186_132-185insGGGCACGCGGGCGTGCAGGACGC (ACADVL) NP_001257376.1:n.132-186_132-185insGGGCACGCGGGCGTGCAGGACGC