Canonical Allele Identifier: CA2576147626

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219804A>C , CM000679.2:g.7219804A>C GRCh38
NC_000017.10:g.7123123A>C , CM000679.1:g.7123123A>C GRCh37
NC_000017.9:g.7063847A>C NCBI36
NG_007975.1:g.4971A>C
NG_008391.2:g.5247T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-955T>G (DLG4) ENSP00000382428.3:n.-955T>G
ENST00000648172.8:c.-955T>G (DLG4) ENSP00000497806.3:n.-955T>G
ENST00000543245.6:c.132-318A>C (ACADVL) ENSP00000438689.2:n.132-318A>C
NM_001270447.1:c.132-318A>C (ACADVL) NP_001257376.1:n.132-318A>C
NM_001365.3:c.-955T>G (DLG4) NP_001356.1:n.-955T>G
XM_005256489.2:c.-955T>G (DLG4) XP_005256546.1:n.-955T>G
XM_011523698.1:c.-955T>G (DLG4) XP_011522000.1:n.-955T>G
XM_011523699.1:c.-225T>G (DLG4) XP_011522001.1:n.-225T>G
XR_243545.2:n.45T>G (DLG4)
XR_934005.1:n.45T>G (DLG4)
NM_001321074.1:c.-955T>G (DLG4) NP_001308003.1:n.-955T>G
NM_001365.4:c.-955T>G (DLG4) NP_001356.1:n.-955T>G
NR_135527.1:n.247T>G (DLG4)
XM_011523699.2:c.-225T>G (DLG4) XP_011522001.1:n.-225T>G
XR_934005.2:n.39T>G (DLG4)
NM_001270447.2:c.132-318A>C (ACADVL) NP_001257376.1:n.132-318A>C