Canonical Allele Identifier: CA2635777886

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219770_7219771del , CM000679.2:g.7219770_7219771del GRCh38
NC_000017.10:g.7123089_7123090del , CM000679.1:g.7123089_7123090del GRCh37
NC_000017.9:g.7063813_7063814del NCBI36
NG_007975.1:g.4937_4938del
NG_008391.2:g.5283_5284del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-919_-918del (DLG4) ENSP00000382428.3:n.-919_-918del
ENST00000648172.8:c.-919_-918del (DLG4) ENSP00000497806.3:n.-919_-918del
ENST00000543245.6:c.132-352_132-351del (ACADVL) ENSP00000438689.2:n.132-352_132-351del
NM_001270447.1:c.132-352_132-351del (ACADVL) NP_001257376.1:n.132-352_132-351del
NM_001365.3:c.-919_-918del (DLG4) NP_001356.1:n.-919_-918del
XM_005256489.2:c.-919_-918del (DLG4) XP_005256546.1:n.-919_-918del
XM_011523698.1:c.-919_-918del (DLG4) XP_011522000.1:n.-919_-918del
XM_011523699.1:c.-189_-188del (DLG4) XP_011522001.1:n.-189_-188del
XR_243545.2:n.81_82del (DLG4)
XR_934005.1:n.81_82del (DLG4)
NM_001321074.1:c.-919_-918del (DLG4) NP_001308003.1:n.-919_-918del
NM_001365.4:c.-919_-918del (DLG4) NP_001356.1:n.-919_-918del
NR_135527.1:n.283_284del (DLG4)
XM_011523699.2:c.-189_-188del (DLG4) XP_011522001.1:n.-189_-188del
XR_934005.2:n.75_76del (DLG4)
NM_001270447.2:c.132-352_132-351del (ACADVL) NP_001257376.1:n.132-352_132-351del