Canonical Allele Identifier: CA1109566982
Gene: DLGAP2 HGNC NCBI

Linked Data

gnomAD v3: 8-1296128-CAG-C
gnomAD v4: 8-1296128-CAG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1296129_1296130del , CM000670.2:g.1296129_1296130del GRCh38
NC_000008.10:g.1244389_1244390del , CM000670.1:g.1244389_1244390del GRCh37
NC_000008.9:g.1231796_1231797del NCBI36
NG_009409.2:g.563411_563412del

Transcript Alleles

HGVS Amino-acid Change
ENST00000421627.7:c.103+37246_103+37247del ENSP00000400258.3:n.103+37246_103+37247del
ENST00000637795.2:c.106+37246_106+37247del MANE Select ENSP00000489774.1:n.106+37246_106+37247del
NR_111948.1:n.2953_2954del
XM_011534761.1:c.-135+37246_-135+37247del XP_011533063.1:n.-135+37246_-135+37247del
XM_011534762.1:c.-135+37246_-135+37247del XP_011533064.1:n.-135+37246_-135+37247del
NM_001346810.1:c.106+37246_106+37247del NP_001333739.1:n.106+37246_106+37247del
NM_001346810.2:c.106+37246_106+37247del MANE Select NP_001333739.1:n.106+37246_106+37247del
Search 100 bp 5'
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