Canonical Allele Identifier: CA863300603
Gene: TOPORS HGNC NCBI

Linked Data

dbSNP Id: rs1239598872
gnomAD v3: 9-32550693-C-G
gnomAD v4: 9-32550693-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32550693C>G , CM000671.2:g.32550693C>G GRCh38
NC_000009.11:g.32550691C>G , CM000671.1:g.32550691C>G GRCh37
NC_000009.10:g.32540691C>G NCBI36
NG_017050.1:g.6932G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.198+81G>C MANE Select ENSP00000353735.2:n.198+81G>C
ENST00000680198.1:c.198+81G>C ENSP00000505143.1:n.198+81G>C
ENST00000681750.1:c.-45+81G>C ENSP00000506413.1:n.-45+81G>C
ENST00000360538.6:c.198+81G>C ENSP00000353735.2:n.198+81G>C
ENST00000379858.1:c.3+1741G>C ENSP00000369187.1:n.3+1741G>C
NM_001195622.1:c.3+1741G>C NP_001182551.1:n.3+1741G>C
NM_005802.4:c.198+81G>C NP_005793.2:n.198+81G>C
NM_005802.5:c.198+81G>C MANE Select NP_005793.2:n.198+81G>C
NM_001195622.2:c.3+1741G>C NP_001182551.1:n.3+1741G>C