Canonical Allele Identifier: CA2685927487

Gene: DLGAP2

Linked Data

• gnomAD v4: 8-1296049-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1296053del , CM000670.2:g.1296053del	GRCh38
NC_000008.10:g.1244313del , CM000670.1:g.1244313del	GRCh37
NC_000008.9:g.1231720del	NCBI36
NG_009409.2:g.563335del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421627.7:c.103+37170del	ENSP00000400258.3:n.103+37170del
ENST00000637795.2:c.106+37170del MANE Select	ENSP00000489774.1:n.106+37170del
NR_111948.1:n.3033del
XM_011534761.1:c.-135+37170del	XP_011533063.1:n.-135+37170del
XM_011534762.1:c.-135+37170del	XP_011533064.1:n.-135+37170del
NM_001346810.1:c.106+37170del	NP_001333739.1:n.106+37170del
NM_001346810.2:c.106+37170del MANE Select	NP_001333739.1:n.106+37170del