Canonical Allele Identifier: CA1844697368

Gene: TOPORS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32550697_32550715delinsGGCGCCGCTCCAGGCGGGA , CM000671.2:g.32550697_32550715delinsGGCGCCGCTCCAGGCGGGA	GRCh38
NC_000009.11:g.32550695_32550713delinsGGCGCCGCTCCAGGCGGGA , CM000671.1:g.32550695_32550713delinsGGCGCCGCTCCAGGCGGGA	GRCh37
NC_000009.10:g.32540695_32540713delinsGGCGCCGCTCCAGGCGGGA	NCBI36
NG_017050.1:g.6910_6928delinsTCCCGCCTGGAGCGGCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC MANE Select	ENSP00000353735.2:n.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC
ENST00000680198.1:c.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC	ENSP00000505143.1:n.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC
ENST00000681750.1:c.-45+59_-45+77delinsTCCCGCCTGGAGCGGCGCC	ENSP00000506413.1:n.-45+59_-45+77delinsTCCCGCCTGGAGCGGCGCC
ENST00000360538.6:c.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC	ENSP00000353735.2:n.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC
ENST00000379858.1:c.3+1719_3+1737delinsTCCCGCCTGGAGCGGCGCC	ENSP00000369187.1:n.3+1719_3+1737delinsTCCCGCCTGGAGCGGCGCC
NM_001195622.1:c.3+1719_3+1737delinsTCCCGCCTGGAGCGGCGCC	NP_001182551.1:n.3+1719_3+1737delinsTCCCGCCTGGAGCGGCGCC
NM_005802.4:c.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC	NP_005793.2:n.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC
NM_005802.5:c.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC MANE Select	NP_005793.2:n.198+59_198+77delinsTCCCGCCTGGAGCGGCGCC
NM_001195622.2:c.3+1719_3+1737delinsTCCCGCCTGGAGCGGCGCC	NP_001182551.1:n.3+1719_3+1737delinsTCCCGCCTGGAGCGGCGCC