Canonical Allele Identifier: CA15628335
Gene: DLG5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2165047

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77791882C>T , CM000672.2:g.77791882C>T GRCh38
NC_000010.10:g.79551640C>T , CM000672.1:g.79551640C>T GRCh37
NC_000010.9:g.79221646C>T NCBI36
NG_011484.1:g.139709G>A

Transcript Alleles

HGVS Amino-acid change
NM_004747.3:c.*558G>A VV NP_004738.3:p.=
XM_005270276.3:c.*558G>A XP_005270333.1:p.=
XM_006718056.2:c.*558G>A XP_006718119.1:p.=
XM_011540341.1:c.*558G>A XP_011538643.1:p.=
XM_011540342.1:c.*558G>A XP_011538644.1:p.=
XM_011540343.1:c.*558G>A XP_011538645.1:p.=
XM_011540344.1:c.*558G>A XP_011538646.1:p.=
XM_011540345.1:c.*558G>A XP_011538647.1:p.=
XM_011540347.1:c.*558G>A XP_011538649.1:p.=
XM_005270276.4:c.*558G>A XP_005270333.1:p.=
XM_006718056.3:c.*558G>A XP_006718119.1:p.=
XM_011540341.3:c.*558G>A XP_011538643.1:p.=
XM_011540344.2:c.*558G>A XP_011538646.1:p.=
XM_011540347.2:c.*558G>A XP_011538649.1:p.=
XM_017016913.1:c.*558G>A XP_016872402.1:p.=
XM_017016914.1:c.*558G>A XP_016872403.1:p.=
XM_017016915.1:c.*558G>A XP_016872404.1:p.=
XM_024448250.1:c.*558G>A XP_024304018.1:p.=
NM_004747.4:c.*558G>A VV MANE Preferred NP_004738.3:p.=
ENST00000372391.6:c.*558G>A ENSP00000361467.2:p.=
ENST00000424842.5:n.3201G>A ENSP00000394797.1:p.=
ENST00000475613.6:n.6155G>A