Canonical Allele Identifier: CA918441466
Gene: TOPORS HGNC NCBI

Linked Data

dbSNP Id: rs1587626724
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32550618_32550622dup , CM000671.2:g.32550618_32550622dup GRCh38
NC_000009.11:g.32550616_32550620dup , CM000671.1:g.32550616_32550620dup GRCh37
NC_000009.10:g.32540616_32540620dup NCBI36
NG_017050.1:g.7004_7008dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.198+153_198+157dup MANE Select ENSP00000353735.2:n.198+153_198+157dup
ENST00000680198.1:c.198+153_198+157dup ENSP00000505143.1:n.198+153_198+157dup
ENST00000681750.1:c.-45+153_-45+157dup ENSP00000506413.1:n.-45+153_-45+157dup
ENST00000360538.6:c.198+153_198+157dup ENSP00000353735.2:n.198+153_198+157dup
ENST00000379858.1:c.3+1813_3+1817dup ENSP00000369187.1:n.3+1813_3+1817dup
NM_001195622.1:c.3+1813_3+1817dup NP_001182551.1:n.3+1813_3+1817dup
NM_005802.4:c.198+153_198+157dup NP_005793.2:n.198+153_198+157dup
NM_005802.5:c.198+153_198+157dup MANE Select NP_005793.2:n.198+153_198+157dup
NM_001195622.2:c.3+1813_3+1817dup NP_001182551.1:n.3+1813_3+1817dup
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