Canonical Allele Identifier: CA774739585

Gene: DLG4 ACADVL

Linked Data

• dbSNP Id: rs1203871186
• gnomAD v4: 17-7219698-G-A
• MyVariant Identifiers: chr17:g.7123017G>A (hg19) ; chr17:g.7219698G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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