Canonical Allele Identifier: CA2635778018

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219830del , CM000679.2:g.7219830del GRCh38
NC_000017.10:g.7123149del , CM000679.1:g.7123149del GRCh37
NC_000017.9:g.7063873del NCBI36
NG_007975.1:g.4997del
NG_008391.2:g.5223del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-979del (DLG4) ENSP00000382428.3:n.-979del
ENST00000648172.8:c.-979del (DLG4) ENSP00000497806.3:n.-979del
ENST00000356839.9:c.-155del (ACADVL) ENSP00000349297.5:n.-155del
ENST00000543245.6:c.132-292del (ACADVL) ENSP00000438689.2:n.132-292del
NM_001270447.1:c.132-292del (ACADVL) NP_001257376.1:n.132-292del
NM_001365.3:c.-979del (DLG4) NP_001356.1:n.-979del
XM_005256489.2:c.-979del (DLG4) XP_005256546.1:n.-979del
XM_011523698.1:c.-979del (DLG4) XP_011522000.1:n.-979del
XR_243545.2:n.21del (DLG4)
XR_934005.1:n.21del (DLG4)
NM_001321074.1:c.-979del (DLG4) NP_001308003.1:n.-979del
NM_001365.4:c.-979del (DLG4) NP_001356.1:n.-979del
NR_135527.1:n.223del (DLG4)
XR_934005.2:n.15del (DLG4)
NM_001270447.2:c.132-292del (ACADVL) NP_001257376.1:n.132-292del