Canonical Allele Identifier: CA464295321
Gene: TOPORS HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.32550886C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.84G>A MANE Select ENSP00000353735.2:p.Arg28=
ENST00000680198.1:c.84G>A ENSP00000505143.1:p.Arg28=
ENST00000681750.1:c.-159G>A ENSP00000506413.1:n.-159G>A
ENST00000360538.6:c.84G>A ENSP00000353735.2:p.Arg28=
ENST00000379858.1:c.3+1546G>A ENSP00000369187.1:n.3+1546G>A
NM_001195622.1:c.3+1546G>A NP_001182551.1:n.3+1546G>A
NM_005802.4:c.84G>A NP_005793.2:p.Arg28=
NM_005802.5:c.84G>A MANE Select NP_005793.2:p.Arg28=
NM_001195622.2:c.3+1546G>A NP_001182551.1:n.3+1546G>A