Canonical Allele Identifier: CA464295438
Gene: TOPORS HGNC NCBI
SMIM27 HGNC NCBI

Linked Data

gnomAD v4: 9-32551164-A-G
MyVariant Identifiers: chr9:g.32551162A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32551164A>G , CM000671.2:g.32551164A>G GRCh38
NC_000009.11:g.32551162A>G , CM000671.1:g.32551162A>G GRCh37
NC_000009.10:g.32541162A>G NCBI36
NG_017050.1:g.6461T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.4-196T>C (TOPORS) MANE Select ENSP00000353735.2:n.4-196T>C
ENST00000453396.5:n.21A>G (SMIM27)
ENST00000680198.1:c.4-196T>C ENSP00000505143.1:n.4-196T>C
ENST00000681750.1:c.-239-196T>C ENSP00000506413.1:n.-239-196T>C
ENST00000360538.6:c.4-196T>C (TOPORS) ENSP00000353735.2:n.4-196T>C
ENST00000379858.1:c.3+1270T>C (TOPORS) ENSP00000369187.1:n.3+1270T>C
NM_001195622.1:c.3+1270T>C (TOPORS) NP_001182551.1:n.3+1270T>C
NM_005802.4:c.4-196T>C (TOPORS) NP_005793.2:n.4-196T>C
NR_033991.1:n.21A>G (SMIM27)
NM_001349118.1:c.-731A>G (SMIM27) NP_001336047.1:n.-731A>G
XM_024447368.1:c.171A>G (SMIM27) XP_024303136.1:p.Gly57=
NM_005802.5:c.4-196T>C (TOPORS) MANE Select NP_005793.2:n.4-196T>C
NM_001195622.2:c.3+1270T>C (TOPORS) NP_001182551.1:n.3+1270T>C