Canonical Allele Identifier: CA2635777918

Linked Data

gnomAD v4: 17-7219788-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219788G>T , CM000679.2:g.7219788G>T GRCh38
NC_000017.10:g.7123107G>T , CM000679.1:g.7123107G>T GRCh37
NC_000017.9:g.7063831G>T NCBI36
NG_007975.1:g.4955G>T
NG_008391.2:g.5263C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399510.8:c.-939C>A (DLG4) ENSP00000382428.3:n.-939C>A
ENST00000648172.8:c.-939C>A (DLG4) ENSP00000497806.3:n.-939C>A
ENST00000543245.6:c.132-334G>T (ACADVL) ENSP00000438689.2:n.132-334G>T
NM_001270447.1:c.132-334G>T (ACADVL) NP_001257376.1:n.132-334G>T
NM_001365.3:c.-939C>A (DLG4) NP_001356.1:n.-939C>A
XM_005256489.2:c.-939C>A (DLG4) XP_005256546.1:n.-939C>A
XM_011523698.1:c.-939C>A (DLG4) XP_011522000.1:n.-939C>A
XM_011523699.1:c.-209C>A (DLG4) XP_011522001.1:n.-209C>A
XR_243545.2:n.61C>A (DLG4)
XR_934005.1:n.61C>A (DLG4)
NM_001321074.1:c.-939C>A (DLG4) NP_001308003.1:n.-939C>A
NM_001365.4:c.-939C>A (DLG4) NP_001356.1:n.-939C>A
NR_135527.1:n.263C>A (DLG4)
XM_011523699.2:c.-209C>A (DLG4) XP_011522001.1:n.-209C>A
XR_934005.2:n.55C>A (DLG4)
NM_001270447.2:c.132-334G>T (ACADVL) NP_001257376.1:n.132-334G>T