Canonical Allele Identifier: CA497693152

Gene: DLG4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7196757C>T , CM000679.2:g.7196757C>T	GRCh38
NC_000017.10:g.7100076C>T , CM000679.1:g.7100076C>T	GRCh37
NC_000017.9:g.7040800C>T	NCBI36
NG_008391.2:g.28294G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001321075.3:c.1083G>A MANE Select	NP_001308004.1:p.Ser361=
ENST00000399506.9:c.1083G>A MANE Select	ENSP00000382425.2:p.Ser361=
NM_001128827.1:c.1074G>A	NP_001122299.1:p.Ser358=
NM_001128827.2:c.1074G>A	NP_001122299.1:p.Ser358=
NM_001128827.3:c.1074G>A	NP_001122299.1:p.Ser358=
NM_001128827.4:c.1074G>A	NP_001122299.1:p.Ser358=
NM_001321074.1:c.1203G>A	NP_001308003.1:p.Ser401=
NM_001321075.1:c.1083G>A	NP_001308004.1:p.Ser361=
NM_001321076.1:c.903G>A	NP_001308005.1:p.Ser301=
NM_001321076.2:c.903G>A	NP_001308005.1:p.Ser301=
NM_001321076.3:c.903G>A	NP_001308005.1:p.Ser301=
NM_001321077.1:c.903G>A	NP_001308006.1:p.Ser301=
NM_001321077.2:c.903G>A	NP_001308006.1:p.Ser301=
NM_001321077.3:c.903G>A	NP_001308006.1:p.Ser301=
NM_001365.3:c.1212G>A	NP_001356.1:p.Ser404=
NM_001365.4:c.1212G>A	NP_001356.1:p.Ser404=
NM_001369566.2:c.1002G>A	NP_001356495.1:p.Ser334=
NM_001369566.3:c.1002G>A	NP_001356495.1:p.Ser334=
NR_135527.1:n.2413G>A
ENST00000302955.10:c.1074G>A	ENSP00000307471.6:p.Ser358=
ENST00000302955.11:c.1074G>A	ENSP00000307471.6:p.Ser358=
ENST00000399506.6:c.1083G>A	ENSP00000382425.2:p.Ser361=
ENST00000399510.6:c.1212G>A	ENSP00000382428.2:p.Ser404=
ENST00000399510.8:c.1203G>A	ENSP00000382428.3:p.Ser401=
ENST00000491753.2:c.1212G>A	ENSP00000467897.2:p.Ser404=
ENST00000648103.1:n.53G>A
ENST00000648103.2:n.1343G>A
ENST00000648172.8:c.1212G>A	ENSP00000497806.3:p.Ser404=
ENST00000648263.1:c.903G>A	ENSP00000498035.1:p.Ser301=
ENST00000648707.1:n.1118G>A
ENST00000648896.1:c.1182G>A	ENSP00000497546.1:p.Ser394=
ENST00000649186.1:c.903G>A	ENSP00000497879.1:p.Ser301=
ENST00000649520.1:c.903G>A	ENSP00000497647.1:p.Ser301=
ENST00000649971.1:c.1002G>A	ENSP00000497011.1:p.Ser334=
ENST00000650120.1:c.903G>A	ENSP00000497553.1:p.Ser301=
XM_005256489.2:c.1203G>A	XP_005256546.1:p.Ser401=
XM_005256491.1:c.1173G>A	XP_005256548.1:p.Ser391=
XM_005256492.1:c.1083G>A	XP_005256549.1:p.Ser361=
XM_005256493.3:c.903G>A	XP_005256550.1:p.Ser301=
XM_005256494.2:c.903G>A	XP_005256551.1:p.Ser301=
XM_011523698.1:c.1302G>A	XP_011522000.1:p.Ser434=
XM_011523699.1:c.1302G>A	XP_011522001.1:p.Ser434=
XM_011523699.2:c.1302G>A	XP_011522001.1:p.Ser434=
XM_011523700.1:c.1095G>A	XP_011522002.1:p.Ser365=
XM_011523701.1:c.1185G>A	XP_011522003.1:p.Ser395=
XM_011523702.1:c.903G>A	XP_011522004.1:p.Ser301=
XM_017024288.2:c.1017G>A	XP_016879777.1:p.Ser339=
XM_017024289.2:c.1008G>A	XP_016879778.1:p.Ser336=
XM_017024290.2:c.1002G>A	XP_016879779.1:p.Ser334=
XM_024450629.1:c.1068G>A	XP_024306397.1:p.Ser356=
XR_243545.2:n.2211G>A
XR_934005.1:n.2301G>A
XR_934005.2:n.2295G>A