Canonical Allele Identifier: CA397718023

Gene: DLG4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7202908G>C , CM000679.2:g.7202908G>C	GRCh38
NC_000017.10:g.7106227G>C , CM000679.1:g.7106227G>C	GRCh37
NC_000017.9:g.7046951G>C	NCBI36
NG_008391.2:g.22143C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001321075.3:c.782C>G MANE Select	NP_001308004.1:p.Thr261Arg
ENST00000399506.9:c.782C>G MANE Select	ENSP00000382425.2:p.Thr261Arg
NM_001128827.1:c.773C>G	NP_001122299.1:p.Thr258Arg
NM_001128827.2:c.773C>G	NP_001122299.1:p.Thr258Arg
NM_001128827.3:c.773C>G	NP_001122299.1:p.Thr258Arg
NM_001128827.4:c.773C>G	NP_001122299.1:p.Thr258Arg
NM_001321074.1:c.902C>G	NP_001308003.1:p.Thr301Arg
NM_001321075.1:c.782C>G	NP_001308004.1:p.Thr261Arg
NM_001321076.1:c.602C>G	NP_001308005.1:p.Thr201Arg
NM_001321076.2:c.602C>G	NP_001308005.1:p.Thr201Arg
NM_001321076.3:c.602C>G	NP_001308005.1:p.Thr201Arg
NM_001321077.1:c.602C>G	NP_001308006.1:p.Thr201Arg
NM_001321077.2:c.602C>G	NP_001308006.1:p.Thr201Arg
NM_001321077.3:c.602C>G	NP_001308006.1:p.Thr201Arg
NM_001365.3:c.911C>G	NP_001356.1:p.Thr304Arg
NM_001365.4:c.911C>G	NP_001356.1:p.Thr304Arg
NM_001369566.2:c.701C>G	NP_001356495.1:p.Thr234Arg
NM_001369566.3:c.701C>G	NP_001356495.1:p.Thr234Arg
NR_135527.1:n.2112C>G
ENST00000302955.10:c.773C>G	ENSP00000307471.6:p.Thr258Arg
ENST00000302955.11:c.773C>G	ENSP00000307471.6:p.Thr258Arg
ENST00000399506.6:c.782C>G	ENSP00000382425.2:p.Thr261Arg
ENST00000399510.6:c.911C>G	ENSP00000382428.2:p.Thr304Arg
ENST00000399510.8:c.902C>G	ENSP00000382428.3:p.Thr301Arg
ENST00000451807.7:c.698C>G	ENSP00000407918.3:p.Thr233Arg
ENST00000485100.5:c.773C>G	ENSP00000460625.1:p.Thr258Arg
ENST00000491753.2:c.911C>G	ENSP00000467897.2:p.Thr304Arg
ENST00000647975.1:c.716C>G	ENSP00000497912.1:p.Thr239Arg
ENST00000648103.2:n.1042C>G
ENST00000648172.8:c.911C>G	ENSP00000497806.3:p.Thr304Arg
ENST00000648263.1:c.602C>G	ENSP00000498035.1:p.Thr201Arg
ENST00000648707.1:n.817C>G
ENST00000648896.1:c.881C>G	ENSP00000497546.1:p.Thr294Arg
ENST00000649186.1:c.602C>G	ENSP00000497879.1:p.Thr201Arg
ENST00000649520.1:c.602C>G	ENSP00000497647.1:p.Thr201Arg
ENST00000649971.1:c.701C>G	ENSP00000497011.1:p.Thr234Arg
ENST00000650120.1:c.602C>G	ENSP00000497553.1:p.Thr201Arg
XM_005256489.2:c.902C>G	XP_005256546.1:p.Thr301Arg
XM_005256491.1:c.872C>G	XP_005256548.1:p.Thr291Arg
XM_005256492.1:c.782C>G	XP_005256549.1:p.Thr261Arg
XM_005256493.3:c.602C>G	XP_005256550.1:p.Thr201Arg
XM_005256494.2:c.602C>G	XP_005256551.1:p.Thr201Arg
XM_011523698.1:c.1001C>G	XP_011522000.1:p.Thr334Arg
XM_011523699.1:c.1001C>G	XP_011522001.1:p.Thr334Arg
XM_011523699.2:c.1001C>G	XP_011522001.1:p.Thr334Arg
XM_011523700.1:c.794C>G	XP_011522002.1:p.Thr265Arg
XM_011523701.1:c.884C>G	XP_011522003.1:p.Thr295Arg
XM_011523702.1:c.602C>G	XP_011522004.1:p.Thr201Arg
XM_017024288.2:c.716C>G	XP_016879777.1:p.Thr239Arg
XM_017024289.2:c.707C>G	XP_016879778.1:p.Thr236Arg
XM_017024290.2:c.701C>G	XP_016879779.1:p.Thr234Arg
XM_024450629.1:c.767C>G	XP_024306397.1:p.Thr256Arg
XR_243545.2:n.1910C>G
XR_934005.1:n.2000C>G
XR_934005.2:n.1994C>G