Canonical Allele Identifier: CA397716167

Gene: DLG4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7196326G>A , CM000679.2:g.7196326G>A	GRCh38
NC_000017.10:g.7099645G>A , CM000679.1:g.7099645G>A	GRCh37
NC_000017.9:g.7040369G>A	NCBI36
NG_008391.2:g.28725C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001321075.3:c.1195C>T MANE Select	NP_001308004.1:p.Arg399Ter
ENST00000399506.9:c.1195C>T MANE Select	ENSP00000382425.2:p.Arg399Ter
NM_001128827.1:c.1186C>T	NP_001122299.1:p.Arg396Ter
NM_001128827.2:c.1186C>T	NP_001122299.1:p.Arg396Ter
NM_001128827.3:c.1186C>T	NP_001122299.1:p.Arg396Ter
NM_001128827.4:c.1186C>T	NP_001122299.1:p.Arg396Ter
NM_001321074.1:c.1315C>T	NP_001308003.1:p.Arg439Ter
NM_001321075.1:c.1195C>T	NP_001308004.1:p.Arg399Ter
NM_001321076.1:c.1015C>T	NP_001308005.1:p.Arg339Ter
NM_001321076.2:c.1015C>T	NP_001308005.1:p.Arg339Ter
NM_001321076.3:c.1015C>T	NP_001308005.1:p.Arg339Ter
NM_001321077.1:c.1015C>T	NP_001308006.1:p.Arg339Ter
NM_001321077.2:c.1015C>T	NP_001308006.1:p.Arg339Ter
NM_001321077.3:c.1015C>T	NP_001308006.1:p.Arg339Ter
NM_001365.3:c.1324C>T	NP_001356.1:p.Arg442Ter
NM_001365.4:c.1324C>T	NP_001356.1:p.Arg442Ter
NM_001369566.2:c.1114C>T	NP_001356495.1:p.Arg372Ter
NM_001369566.3:c.1114C>T	NP_001356495.1:p.Arg372Ter
NR_135527.1:n.2525C>T
ENST00000302955.10:c.1186C>T	ENSP00000307471.6:p.Arg396Ter
ENST00000302955.11:c.1186C>T	ENSP00000307471.6:p.Arg396Ter
ENST00000399506.6:c.1195C>T	ENSP00000382425.2:p.Arg399Ter
ENST00000399510.6:c.1324C>T	ENSP00000382428.2:p.Arg442Ter
ENST00000399510.8:c.1315C>T	ENSP00000382428.3:p.Arg439Ter
ENST00000491753.2:c.1324C>T	ENSP00000467897.2:p.Arg442Ter
ENST00000648103.1:n.165C>T
ENST00000648103.2:n.1455C>T
ENST00000648172.8:c.1324C>T	ENSP00000497806.3:p.Arg442Ter
ENST00000648263.1:c.1015C>T	ENSP00000498035.1:p.Arg339Ter
ENST00000648707.1:n.1230C>T
ENST00000648896.1:c.1294C>T	ENSP00000497546.1:p.Arg432Ter
ENST00000649186.1:c.1015C>T	ENSP00000497879.1:p.Arg339Ter
ENST00000649520.1:c.1015C>T	ENSP00000497647.1:p.Arg339Ter
ENST00000649971.1:c.1114C>T	ENSP00000497011.1:p.Arg372Ter
ENST00000650120.1:c.1015C>T	ENSP00000497553.1:p.Arg339Ter
XM_005256489.2:c.1315C>T	XP_005256546.1:p.Arg439Ter
XM_005256491.1:c.1285C>T	XP_005256548.1:p.Arg429Ter
XM_005256492.1:c.1195C>T	XP_005256549.1:p.Arg399Ter
XM_005256493.3:c.1015C>T	XP_005256550.1:p.Arg339Ter
XM_005256494.2:c.1015C>T	XP_005256551.1:p.Arg339Ter
XM_011523698.1:c.1414C>T	XP_011522000.1:p.Arg472Ter
XM_011523699.1:c.1414C>T	XP_011522001.1:p.Arg472Ter
XM_011523699.2:c.1414C>T	XP_011522001.1:p.Arg472Ter
XM_011523700.1:c.1207C>T	XP_011522002.1:p.Arg403Ter
XM_011523701.1:c.1297C>T	XP_011522003.1:p.Arg433Ter
XM_011523702.1:c.1015C>T	XP_011522004.1:p.Arg339Ter
XM_017024288.2:c.1129C>T	XP_016879777.1:p.Arg377Ter
XM_017024289.2:c.1120C>T	XP_016879778.1:p.Arg374Ter
XM_017024290.2:c.1114C>T	XP_016879779.1:p.Arg372Ter
XM_024450629.1:c.1180C>T	XP_024306397.1:p.Arg394Ter
XR_243545.2:n.2323C>T
XR_934005.1:n.2413C>T
XR_934005.2:n.2407C>T