Canonical Allele Identifier: CA397717980

Gene: DLG4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7202899T>C , CM000679.2:g.7202899T>C	GRCh38
NC_000017.10:g.7106218T>C , CM000679.1:g.7106218T>C	GRCh37
NC_000017.9:g.7046942T>C	NCBI36
NG_008391.2:g.22152A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001321075.3:c.787+4A>G MANE Select	NP_001308004.1:n.787+4A>G
ENST00000399506.9:c.787+4A>G MANE Select	ENSP00000382425.2:n.787+4A>G
NM_001128827.1:c.778+4A>G	NP_001122299.1:n.778+4A>G
NM_001128827.2:c.778+4A>G	NP_001122299.1:n.778+4A>G
NM_001128827.3:c.778+4A>G	NP_001122299.1:n.778+4A>G
NM_001128827.4:c.778+4A>G	NP_001122299.1:n.778+4A>G
NM_001321074.1:c.907+4A>G	NP_001308003.1:n.907+4A>G
NM_001321075.1:c.787+4A>G	NP_001308004.1:n.787+4A>G
NM_001321076.1:c.607+4A>G	NP_001308005.1:n.607+4A>G
NM_001321076.2:c.607+4A>G	NP_001308005.1:n.607+4A>G
NM_001321076.3:c.607+4A>G	NP_001308005.1:n.607+4A>G
NM_001321077.1:c.607+4A>G	NP_001308006.1:n.607+4A>G
NM_001321077.2:c.607+4A>G	NP_001308006.1:n.607+4A>G
NM_001321077.3:c.607+4A>G	NP_001308006.1:n.607+4A>G
NM_001365.3:c.916+4A>G	NP_001356.1:n.916+4A>G
NM_001365.4:c.916+4A>G	NP_001356.1:n.916+4A>G
NM_001369566.2:c.706+4A>G	NP_001356495.1:n.706+4A>G
NM_001369566.3:c.706+4A>G	NP_001356495.1:n.706+4A>G
NR_135527.1:n.2117+4A>G
ENST00000302955.10:c.778+4A>G	ENSP00000307471.6:n.778+4A>G
ENST00000302955.11:c.778+4A>G	ENSP00000307471.6:n.778+4A>G
ENST00000399506.6:c.787+4A>G	ENSP00000382425.2:n.787+4A>G
ENST00000399510.6:c.916+4A>G	ENSP00000382428.2:n.916+4A>G
ENST00000399510.8:c.907+4A>G	ENSP00000382428.3:n.907+4A>G
ENST00000451807.7:c.703+4A>G	ENSP00000407918.3:n.703+4A>G
ENST00000485100.5:c.782A>G	ENSP00000460625.1:p.Glu261Gly
ENST00000491753.2:c.916+4A>G	ENSP00000467897.2:n.916+4A>G
ENST00000647975.1:c.725A>G	ENSP00000497912.1:p.Glu242Gly
ENST00000648103.2:n.1047+4A>G
ENST00000648172.8:c.916+4A>G	ENSP00000497806.3:n.916+4A>G
ENST00000648263.1:c.607+4A>G	ENSP00000498035.1:n.607+4A>G
ENST00000648707.1:n.822+4A>G
ENST00000648896.1:c.886+4A>G	ENSP00000497546.1:n.886+4A>G
ENST00000649186.1:c.607+4A>G	ENSP00000497879.1:n.607+4A>G
ENST00000649520.1:c.607+4A>G	ENSP00000497647.1:n.607+4A>G
ENST00000649971.1:c.706+4A>G	ENSP00000497011.1:n.706+4A>G
ENST00000650120.1:c.607+4A>G	ENSP00000497553.1:n.607+4A>G
XM_005256489.2:c.907+4A>G	XP_005256546.1:n.907+4A>G
XM_005256491.1:c.877+4A>G	XP_005256548.1:n.877+4A>G
XM_005256492.1:c.787+4A>G	XP_005256549.1:n.787+4A>G
XM_005256493.3:c.607+4A>G	XP_005256550.1:n.607+4A>G
XM_005256494.2:c.607+4A>G	XP_005256551.1:n.607+4A>G
XM_011523698.1:c.1006+4A>G	XP_011522000.1:n.1006+4A>G
XM_011523699.1:c.1006+4A>G	XP_011522001.1:n.1006+4A>G
XM_011523699.2:c.1006+4A>G	XP_011522001.1:n.1006+4A>G
XM_011523700.1:c.799+4A>G	XP_011522002.1:n.799+4A>G
XM_011523701.1:c.889+4A>G	XP_011522003.1:n.889+4A>G
XM_011523702.1:c.607+4A>G	XP_011522004.1:n.607+4A>G
XM_017024288.2:c.721+4A>G	XP_016879777.1:n.721+4A>G
XM_017024289.2:c.712+4A>G	XP_016879778.1:n.712+4A>G
XM_017024290.2:c.706+4A>G	XP_016879779.1:n.706+4A>G
XM_024450629.1:c.772+4A>G	XP_024306397.1:n.772+4A>G
XR_243545.2:n.1915+4A>G
XR_934005.1:n.2005+4A>G
XR_934005.2:n.1999+4A>G