Canonical Allele Identifier: CA1109566945

Gene: DLGAP2

Linked Data

• dbSNP Id: rs1800166028
• gnomAD v3: 8-1296104-GTTGA-G
• gnomAD v4: 8-1296104-GTTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1296107_1296110del , CM000670.2:g.1296107_1296110del	GRCh38
NC_000008.10:g.1244367_1244370del , CM000670.1:g.1244367_1244370del	GRCh37
NC_000008.9:g.1231774_1231777del	NCBI36
NG_009409.2:g.563389_563392del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421627.7:c.103+37224_103+37227del	ENSP00000400258.3:n.103+37224_103+37227del
ENST00000637795.2:c.106+37224_106+37227del MANE Select	ENSP00000489774.1:n.106+37224_106+37227del
NR_111948.1:n.2975_2978del
XM_011534761.1:c.-135+37224_-135+37227del	XP_011533063.1:n.-135+37224_-135+37227del
XM_011534762.1:c.-135+37224_-135+37227del	XP_011533064.1:n.-135+37224_-135+37227del
NM_001346810.1:c.106+37224_106+37227del	NP_001333739.1:n.106+37224_106+37227del
NM_001346810.2:c.106+37224_106+37227del MANE Select	NP_001333739.1:n.106+37224_106+37227del