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_000011.8:g.84095494T>C NCBI36
NC_000011.9:g.84417846T>C , CM000673.1:g.84417846T>C GRCh37
NG_021375.1:g.925469A>G

Transcript Alleles

HGVS Amino-acid change
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.=
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.=