Canonical Allele Identifier: CA2245697177

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219808G= , CM000679.2:g.7219808G= GRCh38
NC_000017.10:g.7123127G= , CM000679.1:g.7123127G= GRCh37
NC_000017.9:g.7063851G= NCBI36
NG_007975.1:g.4975G=
NG_008391.2:g.5243C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-959C= (DLG4) ENSP00000382428.3:n.-959C=
ENST00000648172.8:c.-959C= (DLG4) ENSP00000497806.3:n.-959C=
ENST00000356839.9:c.-177G= (ACADVL) ENSP00000349297.5:n.-177G=
ENST00000543245.6:c.132-314G= (ACADVL) ENSP00000438689.2:n.132-314G=
NM_001270447.1:c.132-314G= (ACADVL) NP_001257376.1:n.132-314G=
NM_001365.3:c.-959C= (DLG4) NP_001356.1:n.-959C=
XM_005256489.2:c.-959C= (DLG4) XP_005256546.1:n.-959C=
XM_011523698.1:c.-959C= (DLG4) XP_011522000.1:n.-959C=
XM_011523699.1:c.-229C= (DLG4) XP_011522001.1:n.-229C=
XR_243545.2:n.41C= (DLG4)
XR_934005.1:n.41C= (DLG4)
NM_001321074.1:c.-959C= (DLG4) NP_001308003.1:n.-959C=
NM_001365.4:c.-959C= (DLG4) NP_001356.1:n.-959C=
NR_135527.1:n.243C= (DLG4)
XM_011523699.2:c.-229C= (DLG4) XP_011522001.1:n.-229C=
XR_934005.2:n.35C= (DLG4)
NM_001270447.2:c.132-314G= (ACADVL) NP_001257376.1:n.132-314G=