Canonical Allele Identifier: CA2281257717

Gene: DLGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.3942698_3942725delinsAATCTGTTCTGGGCTTTTGCTTTCCTGG , CM000680.2:g.3942698_3942725delinsAATCTGTTCTGGGCTTTTGCTTTCCTGG	GRCh38
NC_000018.9:g.3942698_3942725delinsAATCTGTTCTGGGCTTTTGCTTTCCTGG , CM000680.1:g.3942698_3942725delinsAATCTGTTCTGGGCTTTTGCTTTCCTGG	GRCh37
NC_000018.8:g.3932698_3932725delinsAATCTGTTCTGGGCTTTTGCTTTCCTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315677.8:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT MANE Select	ENSP00000316377.3:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGC...
ENST00000639615.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	ENSP00000491005.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGC...
ENST00000315677.7:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	ENSP00000316377.3:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGC...
ENST00000581527.5:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	ENSP00000463864.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGC...
ENST00000584874.5:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	ENSP00000462882.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGC...
NM_001242761.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_001229690.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
NM_004746.3:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_004737.2:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAA...
XM_005258171.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_005258228.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XM_005258172.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_005258229.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XM_011525770.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_011524072.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XM_011525771.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_011524073.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XR_935073.1:n.499+62391_499+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT
XM_005258171.3:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_005258228.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XM_011525770.3:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_011524072.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XM_011525771.3:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_011524073.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
XM_024451288.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	XP_024307056.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
NM_004746.4:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT MANE Select	NP_004737.2:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAA...
NM_001242761.2:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_001229690.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
NM_001398525.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_001385454.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
NM_001398526.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_001385455.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
NM_001398527.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_001385456.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...
NM_001398528.1:c.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCAGAACAGATT	NP_001385457.1:n.-73+62391_-73+62418delinsCCAGGAAAGCAAAAGCCCA...