Canonical Allele Identifier: CA226266843

Gene: DLG2

Linked Data

• dbSNP Id: rs17148090
• MyVariant Identifiers: chr11:g.85306432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.85306432A>C , CM000673.2:g.85306432A>C	GRCh38
NC_000011.9:g.85017476A>C , CM000673.1:g.85017476A>C	GRCh37
NC_000011.8:g.84695124A>C	NCBI36
NG_021375.1:g.325839T>G
NG_021375.2:g.327104T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000705960.1:n.398-21067T>G
ENST00000706006.1:c.152-21067T>G	ENSP00000516200.1:n.152-21067T>G
ENST00000706007.1:c.310-21067T>G	ENSP00000516201.1:n.310-21067T>G
ENST00000706205.1:n.353-21067T>G
ENST00000706226.1:c.152-21067T>G	ENSP00000516284.1:n.152-21067T>G
ENST00000706233.1:c.152-21067T>G	ENSP00000516288.1:n.152-21067T>G
ENST00000376104.7:c.41-21067T>G MANE Select	ENSP00000365272.2:n.41-21067T>G
ENST00000650630.1:c.152-21067T>G	ENSP00000497771.1:n.152-21067T>G
ENST00000376104.6:c.41-21067T>G	ENSP00000365272.2:n.41-21067T>G
NM_001142699.1:c.41-21067T>G	NP_001136171.1:n.41-21067T>G
XM_011544778.1:c.190+2553T>G	XP_011543080.1:n.190+2553T>G
XM_011544779.1:c.152-21067T>G	XP_011543081.1:n.152-21067T>G
XM_011544780.1:c.190+2553T>G	XP_011543082.1:n.190+2553T>G
XM_011544781.1:c.190+2553T>G	XP_011543083.1:n.190+2553T>G
XM_011544786.1:c.190+2553T>G	XP_011543088.1:n.190+2553T>G
NM_001351274.1:c.152-21067T>G	NP_001338203.1:n.152-21067T>G
NM_001351275.1:c.152-21067T>G	NP_001338204.1:n.152-21067T>G
XM_011544778.3:c.190+2553T>G	XP_011543080.1:n.190+2553T>G
XM_011544780.3:c.190+2553T>G	XP_011543082.1:n.190+2553T>G
XM_017017254.2:c.190+2553T>G	XP_016872743.1:n.190+2553T>G
XM_017017255.2:c.152-21067T>G	XP_016872744.1:n.152-21067T>G
XM_017017256.2:c.152-21067T>G	XP_016872745.1:n.152-21067T>G
XM_017017257.2:c.152-21067T>G	XP_016872746.1:n.152-21067T>G
XM_017017258.1:c.29-21067T>G	XP_016872747.1:n.29-21067T>G
XM_017017261.2:c.190+2553T>G	XP_016872750.1:n.190+2553T>G
XM_024448378.1:c.152-21067T>G	XP_024304146.1:n.152-21067T>G
XM_024448379.1:c.152-21067T>G	XP_024304147.1:n.152-21067T>G
NM_001351274.2:c.152-21067T>G	NP_001338203.1:n.152-21067T>G
NM_001142699.3:c.41-21067T>G MANE Select	NP_001136171.1:n.41-21067T>G
NM_001351275.2:c.152-21067T>G	NP_001338204.1:n.152-21067T>G