Canonical Allele Identifier: CA2573054557
Community Standard Title: NM_001321075.3(DLG4):c.1855del (p.Val619TrpfsTer?)
Gene: DLG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7192957del , CM000679.2:g.7192957del GRCh38
NC_000017.10:g.7096276del , CM000679.1:g.7096276del GRCh37
NC_000017.9:g.7037000del NCBI36
NG_008391.2:g.32095del

Transcript Alleles

HGVS Amino-acid Change
NM_001321075.3:c.1855del MANE Select NP_001308004.1:p.Val619TrpfsTer?
ENST00000399506.9:c.1855del MANE Select ENSP00000382425.2:p.Val619TrpfsTer?
NM_001128827.1:c.1846del NP_001122299.1:p.Val616TrpfsTer?
NM_001128827.2:c.1846del NP_001122299.1:p.Val616TrpfsTer?
NM_001128827.3:c.1846del NP_001122299.1:p.Val616TrpfsTer?
NM_001128827.4:c.1846del NP_001122299.1:p.Val616TrpfsTer?
NM_001321074.1:c.1975del NP_001308003.1:p.Val659TrpfsTer?
NM_001321075.1:c.1855del NP_001308004.1:p.Val619TrpfsTer?
NM_001321076.1:c.1675del NP_001308005.1:p.Val559TrpfsTer?
NM_001321076.2:c.1675del NP_001308005.1:p.Val559TrpfsTer?
NM_001321076.3:c.1675del NP_001308005.1:p.Val559TrpfsTer?
NM_001321077.1:c.1675del NP_001308006.1:p.Val559TrpfsTer?
NM_001321077.2:c.1675del NP_001308006.1:p.Val559TrpfsTer?
NM_001321077.3:c.1675del NP_001308006.1:p.Val559TrpfsTer?
NM_001365.3:c.1984del NP_001356.1:p.Val662TrpfsTer?
NM_001365.4:c.1984del NP_001356.1:p.Val662TrpfsTer?
NM_001369566.2:c.1774del NP_001356495.1:p.Val592TrpfsTer?
NM_001369566.3:c.1774del NP_001356495.1:p.Val592TrpfsTer?
NR_135527.1:n.3185del
ENST00000302955.10:c.1846del ENSP00000307471.6:p.Val616TrpfsTer?
ENST00000302955.11:c.1846del ENSP00000307471.6:p.Val616TrpfsTer?
ENST00000399506.6:c.1855del ENSP00000382425.2:p.Val619TrpfsTer?
ENST00000399510.6:c.1984del ENSP00000382428.2:p.Val662TrpfsTer?
ENST00000399510.8:c.1975del ENSP00000382428.3:p.Val659TrpfsTer?
ENST00000491753.1:c.237del
ENST00000491753.2:c.1984del ENSP00000467897.2:p.Val662TrpfsTer?
ENST00000648103.1:n.1143del
ENST00000648103.2:n.2433del
ENST00000648172.8:c.1984del ENSP00000497806.3:p.Val662TrpfsTer?
ENST00000648707.1:n.1890del
ENST00000648896.1:c.1954del ENSP00000497546.1:p.Val652TrpfsTer?
ENST00000649186.1:c.1675del ENSP00000497879.1:p.Val559TrpfsTer?
ENST00000649520.1:c.1675del ENSP00000497647.1:p.Val559TrpfsTer?
ENST00000649971.1:c.1774del ENSP00000497011.1:p.Val592TrpfsTer?
ENST00000650120.1:c.1675del ENSP00000497553.1:p.Val559TrpfsTer?
XM_005256489.2:c.1975del XP_005256546.1:p.Val659TrpfsTer?
XM_005256491.1:c.1945del XP_005256548.1:p.Val649TrpfsTer?
XM_005256492.1:c.1855del XP_005256549.1:p.Val619TrpfsTer?
XM_005256493.3:c.1675del XP_005256550.1:p.Val559TrpfsTer?
XM_005256494.2:c.1675del XP_005256551.1:p.Val559TrpfsTer?
XM_011523698.1:c.2074del XP_011522000.1:p.Val692TrpfsTer?
XM_011523699.1:c.2074del XP_011522001.1:p.Val692TrpfsTer?
XM_011523699.2:c.2074del XP_011522001.1:p.Val692TrpfsTer?
XM_011523700.1:c.1867del XP_011522002.1:p.Val623TrpfsTer?
XM_011523701.1:c.1957del XP_011522003.1:p.Val653TrpfsTer?
XM_011523702.1:c.1675del XP_011522004.1:p.Val559TrpfsTer?
XM_017024288.2:c.1789del XP_016879777.1:p.Val597TrpfsTer?
XM_017024289.2:c.1780del XP_016879778.1:p.Val594TrpfsTer?
XM_017024290.2:c.1774del XP_016879779.1:p.Val592TrpfsTer?
XM_024450629.1:c.1840del XP_024306397.1:p.Val614TrpfsTer?
XR_243545.2:n.2983del
XR_934005.1:n.3073del
XR_934005.2:n.3067del