Canonical Allele Identifier: CA1109566975
Gene: DLGAP2 HGNC NCBI

Linked Data

gnomAD v3: 8-1296124-TTTG-T
gnomAD v4: 8-1296124-TTTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1296125_1296127del , CM000670.2:g.1296125_1296127del GRCh38
NC_000008.10:g.1244385_1244387del , CM000670.1:g.1244385_1244387del GRCh37
NC_000008.9:g.1231792_1231794del NCBI36
NG_009409.2:g.563407_563409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000421627.7:c.103+37242_103+37244del ENSP00000400258.3:n.103+37242_103+37244del
ENST00000637795.2:c.106+37242_106+37244del MANE Select ENSP00000489774.1:n.106+37242_106+37244del
NR_111948.1:n.2956_2958del
XM_011534761.1:c.-135+37242_-135+37244del XP_011533063.1:n.-135+37242_-135+37244del
XM_011534762.1:c.-135+37242_-135+37244del XP_011533064.1:n.-135+37242_-135+37244del
NM_001346810.1:c.106+37242_106+37244del NP_001333739.1:n.106+37242_106+37244del
NM_001346810.2:c.106+37242_106+37244del MANE Select NP_001333739.1:n.106+37242_106+37244del
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