Canonical Allele Identifier: CA2635777874

Linked Data

gnomAD v4: 17-7219755-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219755A>C , CM000679.2:g.7219755A>C GRCh38
NC_000017.10:g.7123074A>C , CM000679.1:g.7123074A>C GRCh37
NC_000017.9:g.7063798A>C NCBI36
NG_007975.1:g.4922A>C
NG_008391.2:g.5296T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-906T>G (DLG4) ENSP00000382428.3:n.-906T>G
ENST00000648172.8:c.-906T>G (DLG4) ENSP00000497806.3:n.-906T>G
ENST00000543245.6:c.132-367A>C (ACADVL) ENSP00000438689.2:n.132-367A>C
NM_001270447.1:c.132-367A>C (ACADVL) NP_001257376.1:n.132-367A>C
NM_001365.3:c.-906T>G (DLG4) NP_001356.1:n.-906T>G
XM_005256489.2:c.-906T>G (DLG4) XP_005256546.1:n.-906T>G
XM_011523698.1:c.-906T>G (DLG4) XP_011522000.1:n.-906T>G
XM_011523699.1:c.-176T>G (DLG4) XP_011522001.1:n.-176T>G
XR_243545.2:n.94T>G (DLG4)
XR_934005.1:n.94T>G (DLG4)
NM_001321074.1:c.-906T>G (DLG4) NP_001308003.1:n.-906T>G
NM_001365.4:c.-906T>G (DLG4) NP_001356.1:n.-906T>G
NR_135527.1:n.296T>G (DLG4)
XM_011523699.2:c.-176T>G (DLG4) XP_011522001.1:n.-176T>G
XR_934005.2:n.88T>G (DLG4)
NM_001270447.2:c.132-367A>C (ACADVL) NP_001257376.1:n.132-367A>C