Canonical Allele Identifier: CA8337379

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7217786C>A , CM000679.2:g.7217786C>A GRCh38
NC_000017.10:g.7121105C>A , CM000679.1:g.7121105C>A GRCh37
NC_000017.9:g.7061829C>A NCBI36
NG_007975.1:g.2953C>A
NG_008391.2:g.7265G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.159+455G>T (DLG4) ENSP00000382428.3:n.159+455G>T
ENST00000491753.2:c.159+455G>T (DLG4) ENSP00000467897.2:n.159+455G>T
ENST00000648172.8:c.159+455G>T (DLG4) ENSP00000497806.3:n.159+455G>T
ENST00000648707.1:n.65+455G>T (DLG4)
ENST00000399510.6:c.159+455G>T (DLG4) ENSP00000382428.2:n.159+455G>T
ENST00000543245.6:c.99C>A (ACADVL) ENSP00000438689.2:p.Gly33=
NM_001270447.1:c.99C>A (ACADVL) NP_001257376.1:p.Gly33=
NM_001365.3:c.159+455G>T (DLG4) NP_001356.1:n.159+455G>T
XM_005256489.2:c.159+455G>T (DLG4) XP_005256546.1:n.159+455G>T
XM_011523698.1:c.159+455G>T (DLG4) XP_011522000.1:n.159+455G>T
XM_011523699.1:c.159+455G>T (DLG4) XP_011522001.1:n.159+455G>T
XR_243545.2:n.1158+455G>T (DLG4)
XR_934005.1:n.1158+455G>T (DLG4)
NM_001321074.1:c.159+455G>T (DLG4) NP_001308003.1:n.159+455G>T
NM_001365.4:c.159+455G>T (DLG4) NP_001356.1:n.159+455G>T
NR_135527.1:n.1360+455G>T (DLG4)
XM_011523699.2:c.159+455G>T (DLG4) XP_011522001.1:n.159+455G>T
XR_934005.2:n.1152+455G>T (DLG4)
NM_001270447.2:c.99C>A (ACADVL) NP_001257376.1:p.Gly33=