Canonical Allele Identifier: CA397716469

Gene: DLG4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7196768G>A , CM000679.2:g.7196768G>A	GRCh38
NC_000017.10:g.7100087G>A , CM000679.1:g.7100087G>A	GRCh37
NC_000017.9:g.7040811G>A	NCBI36
NG_008391.2:g.28283C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001321075.3:c.1072C>T MANE Select	NP_001308004.1:p.Gln358Ter
ENST00000399506.9:c.1072C>T MANE Select	ENSP00000382425.2:p.Gln358Ter
NM_001128827.1:c.1063C>T	NP_001122299.1:p.Gln355Ter
NM_001128827.2:c.1063C>T	NP_001122299.1:p.Gln355Ter
NM_001128827.3:c.1063C>T	NP_001122299.1:p.Gln355Ter
NM_001128827.4:c.1063C>T	NP_001122299.1:p.Gln355Ter
NM_001321074.1:c.1192C>T	NP_001308003.1:p.Gln398Ter
NM_001321075.1:c.1072C>T	NP_001308004.1:p.Gln358Ter
NM_001321076.1:c.892C>T	NP_001308005.1:p.Gln298Ter
NM_001321076.2:c.892C>T	NP_001308005.1:p.Gln298Ter
NM_001321076.3:c.892C>T	NP_001308005.1:p.Gln298Ter
NM_001321077.1:c.892C>T	NP_001308006.1:p.Gln298Ter
NM_001321077.2:c.892C>T	NP_001308006.1:p.Gln298Ter
NM_001321077.3:c.892C>T	NP_001308006.1:p.Gln298Ter
NM_001365.3:c.1201C>T	NP_001356.1:p.Gln401Ter
NM_001365.4:c.1201C>T	NP_001356.1:p.Gln401Ter
NM_001369566.2:c.991C>T	NP_001356495.1:p.Gln331Ter
NM_001369566.3:c.991C>T	NP_001356495.1:p.Gln331Ter
NR_135527.1:n.2402C>T
ENST00000302955.10:c.1063C>T	ENSP00000307471.6:p.Gln355Ter
ENST00000302955.11:c.1063C>T	ENSP00000307471.6:p.Gln355Ter
ENST00000399506.6:c.1072C>T	ENSP00000382425.2:p.Gln358Ter
ENST00000399510.6:c.1201C>T	ENSP00000382428.2:p.Gln401Ter
ENST00000399510.8:c.1192C>T	ENSP00000382428.3:p.Gln398Ter
ENST00000491753.2:c.1201C>T	ENSP00000467897.2:p.Gln401Ter
ENST00000648103.1:n.42C>T
ENST00000648103.2:n.1332C>T
ENST00000648172.8:c.1201C>T	ENSP00000497806.3:p.Gln401Ter
ENST00000648263.1:c.892C>T	ENSP00000498035.1:p.Gln298Ter
ENST00000648707.1:n.1107C>T
ENST00000648896.1:c.1171C>T	ENSP00000497546.1:p.Gln391Ter
ENST00000649186.1:c.892C>T	ENSP00000497879.1:p.Gln298Ter
ENST00000649520.1:c.892C>T	ENSP00000497647.1:p.Gln298Ter
ENST00000649971.1:c.991C>T	ENSP00000497011.1:p.Gln331Ter
ENST00000650120.1:c.892C>T	ENSP00000497553.1:p.Gln298Ter
XM_005256489.2:c.1192C>T	XP_005256546.1:p.Gln398Ter
XM_005256491.1:c.1162C>T	XP_005256548.1:p.Gln388Ter
XM_005256492.1:c.1072C>T	XP_005256549.1:p.Gln358Ter
XM_005256493.3:c.892C>T	XP_005256550.1:p.Gln298Ter
XM_005256494.2:c.892C>T	XP_005256551.1:p.Gln298Ter
XM_011523698.1:c.1291C>T	XP_011522000.1:p.Gln431Ter
XM_011523699.1:c.1291C>T	XP_011522001.1:p.Gln431Ter
XM_011523699.2:c.1291C>T	XP_011522001.1:p.Gln431Ter
XM_011523700.1:c.1084C>T	XP_011522002.1:p.Gln362Ter
XM_011523701.1:c.1174C>T	XP_011522003.1:p.Gln392Ter
XM_011523702.1:c.892C>T	XP_011522004.1:p.Gln298Ter
XM_017024288.2:c.1006C>T	XP_016879777.1:p.Gln336Ter
XM_017024289.2:c.997C>T	XP_016879778.1:p.Gln333Ter
XM_017024290.2:c.991C>T	XP_016879779.1:p.Gln331Ter
XM_024450629.1:c.1057C>T	XP_024306397.1:p.Gln353Ter
XR_243545.2:n.2200C>T
XR_934005.1:n.2290C>T
XR_934005.2:n.2284C>T