Canonical Allele Identifier: CA397718856
Community Standard Title: NM_001321075.3(DLG4):c.592G>A (p.Gly198Ser)
Gene: DLG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7203243C>T , CM000679.2:g.7203243C>T GRCh38
NC_000017.10:g.7106562C>T , CM000679.1:g.7106562C>T GRCh37
NC_000017.9:g.7047286C>T NCBI36
NG_008391.2:g.21808G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001321075.3:c.592G>A MANE Select NP_001308004.1:p.Gly198Ser
ENST00000399506.9:c.592G>A MANE Select ENSP00000382425.2:p.Gly198Ser
NM_001128827.1:c.583G>A NP_001122299.1:p.Gly195Ser
NM_001128827.2:c.583G>A NP_001122299.1:p.Gly195Ser
NM_001128827.3:c.583G>A NP_001122299.1:p.Gly195Ser
NM_001128827.4:c.583G>A NP_001122299.1:p.Gly195Ser
NM_001321074.1:c.712G>A NP_001308003.1:p.Gly238Ser
NM_001321075.1:c.592G>A NP_001308004.1:p.Gly198Ser
NM_001321076.1:c.412G>A NP_001308005.1:p.Gly138Ser
NM_001321076.2:c.412G>A NP_001308005.1:p.Gly138Ser
NM_001321076.3:c.412G>A NP_001308005.1:p.Gly138Ser
NM_001321077.1:c.412G>A NP_001308006.1:p.Gly138Ser
NM_001321077.2:c.412G>A NP_001308006.1:p.Gly138Ser
NM_001321077.3:c.412G>A NP_001308006.1:p.Gly138Ser
NM_001365.3:c.721G>A NP_001356.1:p.Gly241Ser
NM_001365.4:c.721G>A NP_001356.1:p.Gly241Ser
NM_001369566.2:c.511G>A NP_001356495.1:p.Gly171Ser
NM_001369566.3:c.511G>A NP_001356495.1:p.Gly171Ser
NR_135527.1:n.1922G>A
ENST00000302955.10:c.583G>A ENSP00000307471.6:p.Gly195Ser
ENST00000302955.11:c.583G>A ENSP00000307471.6:p.Gly195Ser
ENST00000399506.6:c.592G>A ENSP00000382425.2:p.Gly198Ser
ENST00000399510.6:c.721G>A ENSP00000382428.2:p.Gly241Ser
ENST00000399510.8:c.712G>A ENSP00000382428.3:p.Gly238Ser
ENST00000447163.5:c.682G>A ENSP00000388122.1:p.Gly228Ser
ENST00000447163.6:c.682G>A ENSP00000388122.2:p.Gly228Ser
ENST00000451807.6:c.691G>A ENSP00000407918.2:p.Gly231Ser
ENST00000451807.7:c.508G>A ENSP00000407918.3:p.Gly170Ser
ENST00000485100.5:c.583G>A ENSP00000460625.1:p.Gly195Ser
ENST00000486626.8:c.412G>A ENSP00000465720.2:p.Gly138Ser
ENST00000491753.2:c.721G>A ENSP00000467897.2:p.Gly241Ser
ENST00000493294.2:c.499G>A ENSP00000465789.2:p.Gly167Ser
ENST00000647975.1:c.526G>A ENSP00000497912.1:p.Gly176Ser
ENST00000648103.2:n.852G>A
ENST00000648172.8:c.721G>A ENSP00000497806.3:p.Gly241Ser
ENST00000648263.1:c.412G>A ENSP00000498035.1:p.Gly138Ser
ENST00000648707.1:n.627G>A
ENST00000648896.1:c.691G>A ENSP00000497546.1:p.Gly231Ser
ENST00000649186.1:c.412G>A ENSP00000497879.1:p.Gly138Ser
ENST00000649520.1:c.412G>A ENSP00000497647.1:p.Gly138Ser
ENST00000649971.1:c.511G>A ENSP00000497011.1:p.Gly171Ser
ENST00000650120.1:c.412G>A ENSP00000497553.1:p.Gly138Ser
XM_005256489.2:c.712G>A XP_005256546.1:p.Gly238Ser
XM_005256491.1:c.682G>A XP_005256548.1:p.Gly228Ser
XM_005256492.1:c.592G>A XP_005256549.1:p.Gly198Ser
XM_005256493.3:c.412G>A XP_005256550.1:p.Gly138Ser
XM_005256494.2:c.412G>A XP_005256551.1:p.Gly138Ser
XM_011523698.1:c.811G>A XP_011522000.1:p.Gly271Ser
XM_011523699.1:c.811G>A XP_011522001.1:p.Gly271Ser
XM_011523699.2:c.811G>A XP_011522001.1:p.Gly271Ser
XM_011523700.1:c.604G>A XP_011522002.1:p.Gly202Ser
XM_011523701.1:c.694G>A XP_011522003.1:p.Gly232Ser
XM_011523702.1:c.412G>A XP_011522004.1:p.Gly138Ser
XM_017024288.2:c.526G>A XP_016879777.1:p.Gly176Ser
XM_017024289.2:c.517G>A XP_016879778.1:p.Gly173Ser
XM_017024290.2:c.511G>A XP_016879779.1:p.Gly171Ser
XM_024450629.1:c.577G>A XP_024306397.1:p.Gly193Ser
XR_243545.2:n.1720G>A
XR_934005.1:n.1810G>A
XR_934005.2:n.1804G>A