Canonical Allele Identifier: CA2245697110

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219698G= , CM000679.2:g.7219698G= GRCh38
NC_000017.10:g.7123017G= , CM000679.1:g.7123017G= GRCh37
NC_000017.9:g.7063741G= NCBI36
NG_007975.1:g.4865G=
NG_008391.2:g.5353C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-849C= (DLG4) ENSP00000382428.3:n.-849C=
ENST00000491753.2:c.-849C= (DLG4) ENSP00000467897.2:n.-849C=
ENST00000648172.8:c.-849C= (DLG4) ENSP00000497806.3:n.-849C=
ENST00000399510.6:c.-849C= (DLG4) ENSP00000382428.2:n.-849C=
ENST00000543245.6:c.132-424G= (ACADVL) ENSP00000438689.2:n.132-424G=
NM_001270447.1:c.132-424G= (ACADVL) NP_001257376.1:n.132-424G=
NM_001365.3:c.-849C= (DLG4) NP_001356.1:n.-849C=
XM_005256489.2:c.-849C= (DLG4) XP_005256546.1:n.-849C=
XM_011523698.1:c.-849C= (DLG4) XP_011522000.1:n.-849C=
XM_011523699.1:c.-119C= (DLG4) XP_011522001.1:n.-119C=
XR_243545.2:n.151C= (DLG4)
XR_934005.1:n.151C= (DLG4)
NM_001321074.1:c.-849C= (DLG4) NP_001308003.1:n.-849C=
NM_001365.4:c.-849C= (DLG4) NP_001356.1:n.-849C=
NR_135527.1:n.353C= (DLG4)
XM_011523699.2:c.-119C= (DLG4) XP_011522001.1:n.-119C=
XR_934005.2:n.145C= (DLG4)
NM_001270447.2:c.132-424G= (ACADVL) NP_001257376.1:n.132-424G=