Canonical Allele Identifier: CA13445783
Gene: DLG2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10501570

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.84706803T>C , CM000673.2:g.84706803T>C GRCh38
NC_000011.9:g.84417846T>C , CM000673.1:g.84417846T>C GRCh37
NC_000011.8:g.84095494T>C NCBI36
NG_021375.1:g.925469A>G

Transcript Alleles

HGVS Amino-acid change
NM_001142699.1:c.358-172072A>G VV NP_001136171.1:p.=
NM_001300983.1:c.43-172072A>G VV NP_001287912.1:p.=
NM_001364.3:c.43-172072A>G VV NP_001355.2:p.=
XM_005273806.2:c.102+13493A>G XP_005273863.1:p.=
XM_011544778.1:c.508-172072A>G XP_011543080.1:p.=
XM_011544779.1:c.469-172072A>G XP_011543081.1:p.=
XM_011544780.1:c.508-172072A>G XP_011543082.1:p.=
XM_011544781.1:c.433-172072A>G XP_011543083.1:p.=
XM_011544782.1:c.106-172072A>G XP_011543084.1:p.=
XM_011544783.1:c.102+13493A>G XP_011543085.1:p.=
XM_011544784.1:c.43-172075A>G XP_011543086.1:p.=
XM_011544785.1:c.31-172072A>G XP_011543087.1:p.=
XM_011544786.1:c.508-172072A>G XP_011543088.1:p.=
NM_001351274.1:c.394-172072A>G VV NP_001338203.1:p.=
NM_001351275.1:c.394-172075A>G VV NP_001338204.1:p.=
NM_001351276.1:c.102+13493A>G VV NP_001338205.1:p.=
XM_011544778.3:c.508-172072A>G
XM_011544780.3:c.508-172072A>G
XM_011544782.2:c.106-172072A>G
XM_017017254.2:c.508-172072A>G XP_016872743.1:p.=
XM_017017255.2:c.469-172072A>G XP_016872744.1:p.=
XM_017017256.2:c.469-172072A>G XP_016872745.1:p.=
XM_017017257.2:c.469-172075A>G XP_016872746.1:p.=
XM_017017258.1:c.346-172072A>G XP_016872747.1:p.=
XM_017017261.2:c.508-172072A>G XP_016872750.1:p.=
XM_017017263.1:c.106-172072A>G XP_016872752.1:p.=
XM_017017264.2:c.102+13493A>G XP_016872753.1:p.=
XM_017017265.2:c.102+13493A>G XP_016872754.1:p.=
XM_017017267.1:c.43-172072A>G XP_016872756.1:p.=
XM_017017268.1:c.43-172075A>G XP_016872757.1:p.=
XM_017017269.1:c.31-172072A>G XP_016872758.1:p.=
XM_017017270.1:c.106-172072A>G XP_016872759.1:p.=
XM_017017271.2:c.102+13493A>G XP_016872760.1:p.=
XM_017017274.1:c.43-172072A>G XP_016872763.1:p.=
XM_017017276.1:c.31-172072A>G XP_016872765.1:p.=
XM_017017279.1:c.106-172072A>G XP_016872768.1:p.=
XM_017017280.2:c.106-172075A>G XP_016872769.1:p.=
XM_017017281.2:c.102+13493A>G XP_016872770.1:p.=
XM_017017285.1:c.31-172072A>G XP_016872774.1:p.=
XM_024448378.1:c.394-172072A>G XP_024304146.1:p.=
XM_024448379.1:c.394-172075A>G XP_024304147.1:p.=
ENST00000376104.6:c.358-172072A>G ENSP00000365272.2:p.=
ENST00000398309.6:c.43-172072A>G ENSP00000381355.2:p.=
ENST00000524982.5:c.43-172072A>G ENSP00000432894.1:p.=
ENST00000527088.1:c.106-172072A>G ENSP00000435809.1:p.=
ENST00000529111.5:n.321-172072A>G
ENST00000530589.1:n.62-19526A>G
ENST00000532653.5:c.43-172072A>G ENSP00000435849.1:p.=