Canonical Allele Identifier: CA587156159
Gene: TOPORS HGNC NCBI

Linked Data

dbSNP Id: rs1277276568
gnomAD v2: 9-32550722-T-A
gnomAD v4: 9-32550724-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32550724T>A , CM000671.2:g.32550724T>A GRCh38
NC_000009.11:g.32550722T>A , CM000671.1:g.32550722T>A GRCh37
NC_000009.10:g.32540722T>A NCBI36
NG_017050.1:g.6901A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.198+50A>T MANE Select ENSP00000353735.2:n.198+50A>T
ENST00000680198.1:c.198+50A>T ENSP00000505143.1:n.198+50A>T
ENST00000681750.1:c.-45+50A>T ENSP00000506413.1:n.-45+50A>T
ENST00000360538.6:c.198+50A>T ENSP00000353735.2:n.198+50A>T
ENST00000379858.1:c.3+1710A>T ENSP00000369187.1:n.3+1710A>T
NM_001195622.1:c.3+1710A>T NP_001182551.1:n.3+1710A>T
NM_005802.4:c.198+50A>T NP_005793.2:n.198+50A>T
NM_005802.5:c.198+50A>T MANE Select NP_005793.2:n.198+50A>T
NM_001195622.2:c.3+1710A>T NP_001182551.1:n.3+1710A>T