Canonical Allele Identifier: CA1757361165

Gene: DLGAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1296129_1296140delinsAGGGTGGAGTTG , CM000670.2:g.1296129_1296140delinsAGGGTGGAGTTG	GRCh38
NC_000008.10:g.1244389_1244400delinsAGGGTGGAGTTG , CM000670.1:g.1244389_1244400delinsAGGGTGGAGTTG	GRCh37
NC_000008.9:g.1231796_1231807delinsAGGGTGGAGTTG	NCBI36
NG_009409.2:g.563411_563422delinsAGGGTGGAGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421627.7:c.103+37246_103+37257delinsAGGGTGGAGTTG	ENSP00000400258.3:n.103+37246_103+37257delinsAGGGTGGAGTTG
ENST00000637795.2:c.106+37246_106+37257delinsAGGGTGGAGTTG MANE Select	ENSP00000489774.1:n.106+37246_106+37257delinsAGGGTGGAGTTG
NR_111948.1:n.2943_2954delinsCAACTCCACCCT
XM_011534761.1:c.-135+37246_-135+37257delinsAGGGTGGAGTTG	XP_011533063.1:n.-135+37246_-135+37257delinsAGGGTGGAGTTG
XM_011534762.1:c.-135+37246_-135+37257delinsAGGGTGGAGTTG	XP_011533064.1:n.-135+37246_-135+37257delinsAGGGTGGAGTTG
NM_001346810.1:c.106+37246_106+37257delinsAGGGTGGAGTTG	NP_001333739.1:n.106+37246_106+37257delinsAGGGTGGAGTTG
NM_001346810.2:c.106+37246_106+37257delinsAGGGTGGAGTTG MANE Select	NP_001333739.1:n.106+37246_106+37257delinsAGGGTGGAGTTG