Canonical Allele Identifier: CA2245697129

Gene: DLG4 ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7219734A= , CM000679.2:g.7219734A=	GRCh38
NC_000017.10:g.7123053A= , CM000679.1:g.7123053A=	GRCh37
NC_000017.9:g.7063777A=	NCBI36
NG_007975.1:g.4901A=
NG_008391.2:g.5317T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399510.8:c.-885T= (DLG4)	ENSP00000382428.3:n.-885T=
ENST00000491753.2:c.-885T= (DLG4)	ENSP00000467897.2:n.-885T=
ENST00000648172.8:c.-885T= (DLG4)	ENSP00000497806.3:n.-885T=
ENST00000543245.6:c.132-388A= (ACADVL)	ENSP00000438689.2:n.132-388A=
NM_001270447.1:c.132-388A= (ACADVL)	NP_001257376.1:n.132-388A=
NM_001365.3:c.-885T= (DLG4)	NP_001356.1:n.-885T=
XM_005256489.2:c.-885T= (DLG4)	XP_005256546.1:n.-885T=
XM_011523698.1:c.-885T= (DLG4)	XP_011522000.1:n.-885T=
XM_011523699.1:c.-155T= (DLG4)	XP_011522001.1:n.-155T=
XR_243545.2:n.115T= (DLG4)
XR_934005.1:n.115T= (DLG4)
NM_001321074.1:c.-885T= (DLG4)	NP_001308003.1:n.-885T=
NM_001365.4:c.-885T= (DLG4)	NP_001356.1:n.-885T=
NR_135527.1:n.317T= (DLG4)
XM_011523699.2:c.-155T= (DLG4)	XP_011522001.1:n.-155T=
XR_934005.2:n.109T= (DLG4)
NM_001270447.2:c.132-388A= (ACADVL)	NP_001257376.1:n.132-388A=