Canonical Allele Identifier: CA2576147623

Gene: DLG4 ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7219791A>T , CM000679.2:g.7219791A>T	GRCh38
NC_000017.10:g.7123110A>T , CM000679.1:g.7123110A>T	GRCh37
NC_000017.9:g.7063834A>T	NCBI36
NG_007975.1:g.4958A>T
NG_008391.2:g.5260T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399510.8:c.-942T>A (DLG4)	ENSP00000382428.3:n.-942T>A
ENST00000648172.8:c.-942T>A (DLG4)	ENSP00000497806.3:n.-942T>A
ENST00000543245.6:c.132-331A>T (ACADVL)	ENSP00000438689.2:n.132-331A>T
NM_001270447.1:c.132-331A>T (ACADVL)	NP_001257376.1:n.132-331A>T
NM_001365.3:c.-942T>A (DLG4)	NP_001356.1:n.-942T>A
XM_005256489.2:c.-942T>A (DLG4)	XP_005256546.1:n.-942T>A
XM_011523698.1:c.-942T>A (DLG4)	XP_011522000.1:n.-942T>A
XM_011523699.1:c.-212T>A (DLG4)	XP_011522001.1:n.-212T>A
XR_243545.2:n.58T>A (DLG4)
XR_934005.1:n.58T>A (DLG4)
NM_001321074.1:c.-942T>A (DLG4)	NP_001308003.1:n.-942T>A
NM_001365.4:c.-942T>A (DLG4)	NP_001356.1:n.-942T>A
NR_135527.1:n.260T>A (DLG4)
XM_011523699.2:c.-212T>A (DLG4)	XP_011522001.1:n.-212T>A
XR_934005.2:n.52T>A (DLG4)
NM_001270447.2:c.132-331A>T (ACADVL)	NP_001257376.1:n.132-331A>T