Canonical Allele Identifier: CA1844697244

Gene: TOPORS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32550628_32550634delinsGGGCCCT , CM000671.2:g.32550628_32550634delinsGGGCCCT	GRCh38
NC_000009.11:g.32550626_32550632delinsGGGCCCT , CM000671.1:g.32550626_32550632delinsGGGCCCT	GRCh37
NC_000009.10:g.32540626_32540632delinsGGGCCCT	NCBI36
NG_017050.1:g.6991_6997delinsAGGGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.198+140_198+146delinsAGGGCCC MANE Select	ENSP00000353735.2:n.198+140_198+146delinsAGGGCCC
ENST00000680198.1:c.198+140_198+146delinsAGGGCCC	ENSP00000505143.1:n.198+140_198+146delinsAGGGCCC
ENST00000681750.1:c.-45+140_-45+146delinsAGGGCCC	ENSP00000506413.1:n.-45+140_-45+146delinsAGGGCCC
ENST00000360538.6:c.198+140_198+146delinsAGGGCCC	ENSP00000353735.2:n.198+140_198+146delinsAGGGCCC
ENST00000379858.1:c.3+1800_3+1806delinsAGGGCCC	ENSP00000369187.1:n.3+1800_3+1806delinsAGGGCCC
NM_001195622.1:c.3+1800_3+1806delinsAGGGCCC	NP_001182551.1:n.3+1800_3+1806delinsAGGGCCC
NM_005802.4:c.198+140_198+146delinsAGGGCCC	NP_005793.2:n.198+140_198+146delinsAGGGCCC
NM_005802.5:c.198+140_198+146delinsAGGGCCC MANE Select	NP_005793.2:n.198+140_198+146delinsAGGGCCC
NM_001195622.2:c.3+1800_3+1806delinsAGGGCCC	NP_001182551.1:n.3+1800_3+1806delinsAGGGCCC