Canonical Allele Identifier: CA863300608
Gene: TOPORS HGNC NCBI

Linked Data

dbSNP Id: rs1205494939
gnomAD v3: 9-32550765-C-T
gnomAD v4: 9-32550765-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32550765C>T , CM000671.2:g.32550765C>T GRCh38
NC_000009.11:g.32550763C>T , CM000671.1:g.32550763C>T GRCh37
NC_000009.10:g.32540763C>T NCBI36
NG_017050.1:g.6860G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.198+9G>A MANE Select ENSP00000353735.2:n.198+9G>A
ENST00000680198.1:c.198+9G>A ENSP00000505143.1:n.198+9G>A
ENST00000681750.1:c.-45+9G>A ENSP00000506413.1:n.-45+9G>A
ENST00000360538.6:c.198+9G>A ENSP00000353735.2:n.198+9G>A
ENST00000379858.1:c.3+1669G>A ENSP00000369187.1:n.3+1669G>A
NM_001195622.1:c.3+1669G>A NP_001182551.1:n.3+1669G>A
NM_005802.4:c.198+9G>A NP_005793.2:n.198+9G>A
NM_005802.5:c.198+9G>A MANE Select NP_005793.2:n.198+9G>A
NM_001195622.2:c.3+1669G>A NP_001182551.1:n.3+1669G>A