Canonical Allele Identifier: CA2245697198

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219830G= , CM000679.2:g.7219830G= GRCh38
NC_000017.10:g.7123149G= , CM000679.1:g.7123149G= GRCh37
NC_000017.9:g.7063873G= NCBI36
NG_007975.1:g.4997G=
NG_008391.2:g.5221C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-981C= (DLG4) ENSP00000382428.3:n.-981C=
ENST00000648172.8:c.-981C= (DLG4) ENSP00000497806.3:n.-981C=
ENST00000356839.9:c.-155G= (ACADVL) ENSP00000349297.5:n.-155G=
ENST00000543245.6:c.132-292G= (ACADVL) ENSP00000438689.2:n.132-292G=
NM_001270447.1:c.132-292G= (ACADVL) NP_001257376.1:n.132-292G=
NM_001365.3:c.-981C= (DLG4) NP_001356.1:n.-981C=
XM_005256489.2:c.-981C= (DLG4) XP_005256546.1:n.-981C=
XM_011523698.1:c.-981C= (DLG4) XP_011522000.1:n.-981C=
XR_243545.2:n.19C= (DLG4)
XR_934005.1:n.19C= (DLG4)
NM_001321074.1:c.-981C= (DLG4) NP_001308003.1:n.-981C=
NM_001365.4:c.-981C= (DLG4) NP_001356.1:n.-981C=
NR_135527.1:n.221C= (DLG4)
XR_934005.2:n.13C= (DLG4)
NM_001270447.2:c.132-292G= (ACADVL) NP_001257376.1:n.132-292G=