Canonical Allele Identifier: CA5020731
Gene: TOPORS HGNC NCBI

Linked Data

dbSNP Id: rs370921947
gnomAD v2: 9-32550886-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32550888C>A , CM000671.2:g.32550888C>A GRCh38
NC_000009.11:g.32550886C>A , CM000671.1:g.32550886C>A GRCh37
NC_000009.10:g.32540886C>A NCBI36
NG_017050.1:g.6737G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.84G>T MANE Select ENSP00000353735.2:p.Arg28Ser
ENST00000680198.1:c.84G>T ENSP00000505143.1:p.Arg28Ser
ENST00000681750.1:c.-159G>T ENSP00000506413.1:n.-159G>T
ENST00000360538.6:c.84G>T ENSP00000353735.2:p.Arg28Ser
ENST00000379858.1:c.3+1546G>T ENSP00000369187.1:n.3+1546G>T
NM_001195622.1:c.3+1546G>T NP_001182551.1:n.3+1546G>T
NM_005802.4:c.84G>T NP_005793.2:p.Arg28Ser
NM_005802.5:c.84G>T MANE Select NP_005793.2:p.Arg28Ser
NM_001195622.2:c.3+1546G>T NP_001182551.1:n.3+1546G>T