Canonical Allele Identifier: CA15717505

Gene: DLG2

Linked Data

• dbSNP Id: rs10898392
• gnomAD v2: 11-85164751-G-T
• gnomAD v3: 11-85453707-G-T
• gnomAD v4: 11-85453707-G-T
• MyVariant Identifiers: chr11:g.85164751G>T (hg19) ; chr11:g.85453707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.85453707G>T , CM000673.2:g.85453707G>T	GRCh38
NC_000011.9:g.85164751G>T , CM000673.1:g.85164751G>T	GRCh37
NC_000011.8:g.84842399G>T	NCBI36
NG_021375.1:g.178564C>A
NG_021375.2:g.179829C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000705960.1:n.397+144950C>A
ENST00000706006.1:c.151+144950C>A	ENSP00000516200.1:n.151+144950C>A
ENST00000706007.1:c.309+71284C>A	ENSP00000516201.1:n.309+71284C>A
ENST00000706205.1:n.352+144950C>A
ENST00000706226.1:c.151+144950C>A	ENSP00000516284.1:n.151+144950C>A
ENST00000706233.1:c.151+144950C>A	ENSP00000516288.1:n.151+144950C>A
ENST00000376104.7:c.40+144950C>A MANE Select	ENSP00000365272.2:n.40+144950C>A
ENST00000650630.1:c.151+144950C>A	ENSP00000497771.1:n.151+144950C>A
ENST00000376104.6:c.40+144950C>A	ENSP00000365272.2:n.40+144950C>A
NM_001142699.1:c.40+144950C>A	NP_001136171.1:n.40+144950C>A
XM_011544778.1:c.152-144684C>A	XP_011543080.1:n.152-144684C>A
XM_011544779.1:c.151+144950C>A	XP_011543081.1:n.151+144950C>A
XM_011544780.1:c.152-144684C>A	XP_011543082.1:n.152-144684C>A
XM_011544781.1:c.152-144684C>A	XP_011543083.1:n.152-144684C>A
XM_011544786.1:c.152-144684C>A	XP_011543088.1:n.152-144684C>A
NM_001351274.1:c.151+144950C>A	NP_001338203.1:n.151+144950C>A
NM_001351275.1:c.151+144950C>A	NP_001338204.1:n.151+144950C>A
XM_011544778.3:c.152-144684C>A	XP_011543080.1:n.152-144684C>A
XM_011544780.3:c.152-144684C>A	XP_011543082.1:n.152-144684C>A
XM_017017254.2:c.152-144684C>A	XP_016872743.1:n.152-144684C>A
XM_017017255.2:c.151+144950C>A	XP_016872744.1:n.151+144950C>A
XM_017017256.2:c.151+144950C>A	XP_016872745.1:n.151+144950C>A
XM_017017257.2:c.151+144950C>A	XP_016872746.1:n.151+144950C>A
XM_017017261.2:c.152-144684C>A	XP_016872750.1:n.152-144684C>A
XM_024448378.1:c.151+144950C>A	XP_024304146.1:n.151+144950C>A
XM_024448379.1:c.151+144950C>A	XP_024304147.1:n.151+144950C>A
NM_001351274.2:c.151+144950C>A	NP_001338203.1:n.151+144950C>A
NM_001142699.3:c.40+144950C>A MANE Select	NP_001136171.1:n.40+144950C>A
NM_001351275.2:c.151+144950C>A	NP_001338204.1:n.151+144950C>A