Canonical Allele Identifier: CA2635777919

Linked Data

gnomAD v4: 17-7219789-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219789A>G , CM000679.2:g.7219789A>G GRCh38
NC_000017.10:g.7123108A>G , CM000679.1:g.7123108A>G GRCh37
NC_000017.9:g.7063832A>G NCBI36
NG_007975.1:g.4956A>G
NG_008391.2:g.5262T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-940T>C (DLG4) ENSP00000382428.3:n.-940T>C
ENST00000648172.8:c.-940T>C (DLG4) ENSP00000497806.3:n.-940T>C
ENST00000543245.6:c.132-333A>G (ACADVL) ENSP00000438689.2:n.132-333A>G
NM_001270447.1:c.132-333A>G (ACADVL) NP_001257376.1:n.132-333A>G
NM_001365.3:c.-940T>C (DLG4) NP_001356.1:n.-940T>C
XM_005256489.2:c.-940T>C (DLG4) XP_005256546.1:n.-940T>C
XM_011523698.1:c.-940T>C (DLG4) XP_011522000.1:n.-940T>C
XM_011523699.1:c.-210T>C (DLG4) XP_011522001.1:n.-210T>C
XR_243545.2:n.60T>C (DLG4)
XR_934005.1:n.60T>C (DLG4)
NM_001321074.1:c.-940T>C (DLG4) NP_001308003.1:n.-940T>C
NM_001365.4:c.-940T>C (DLG4) NP_001356.1:n.-940T>C
NR_135527.1:n.262T>C (DLG4)
XM_011523699.2:c.-210T>C (DLG4) XP_011522001.1:n.-210T>C
XR_934005.2:n.54T>C (DLG4)
NM_001270447.2:c.132-333A>G (ACADVL) NP_001257376.1:n.132-333A>G