Canonical Allele Identifier: CA2635778090

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219857del , CM000679.2:g.7219857del GRCh38
NC_000017.10:g.7123176del , CM000679.1:g.7123176del GRCh37
NC_000017.9:g.7063900del NCBI36
NG_007975.1:g.5024del
NG_008391.2:g.5197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-128del (ACADVL) ENSP00000325395.5:n.-128del
ENST00000356839.9:c.-128del (ACADVL) ENSP00000349297.5:n.-128del
ENST00000543245.6:c.132-265del (ACADVL) ENSP00000438689.2:n.132-265del
NM_000018.3:c.-128del (ACADVL) NP_000009.1:n.-128del
NM_001033859.2:c.-128del (ACADVL) NP_001029031.1:n.-128del
NM_001270447.1:c.132-265del (ACADVL) NP_001257376.1:n.132-265del
NM_001270448.1:c.-431del (ACADVL) NP_001257377.1:n.-431del
NM_001365.3:c.-1005del (DLG4) NP_001356.1:n.-1005del
NM_001321074.1:c.-1005del (DLG4) NP_001308003.1:n.-1005del
NM_001365.4:c.-1005del (DLG4) NP_001356.1:n.-1005del
NR_135527.1:n.197del (DLG4)
NM_001270447.2:c.132-265del (ACADVL) NP_001257376.1:n.132-265del