Canonical Allele Identifier: CA192366205
Gene: TOPORS HGNC NCBI
SMIM27 HGNC NCBI

Linked Data

dbSNP Id: rs183953517
gnomAD v2: 9-32551209-T-G
gnomAD v3: 9-32551211-T-G
gnomAD v4: 9-32551211-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32551211T>G , CM000671.2:g.32551211T>G GRCh38
NC_000009.11:g.32551209T>G , CM000671.1:g.32551209T>G GRCh37
NC_000009.10:g.32541209T>G NCBI36
NG_017050.1:g.6414A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.4-243A>C (TOPORS) MANE Select ENSP00000353735.2:n.4-243A>C
ENST00000453396.5:n.68T>G (SMIM27)
ENST00000680198.1:c.4-243A>C ENSP00000505143.1:n.4-243A>C
ENST00000681750.1:c.-240+154A>C ENSP00000506413.1:n.-240+154A>C
ENST00000360538.6:c.4-243A>C (TOPORS) ENSP00000353735.2:n.4-243A>C
ENST00000379858.1:c.3+1223A>C (TOPORS) ENSP00000369187.1:n.3+1223A>C
NM_001195622.1:c.3+1223A>C (TOPORS) NP_001182551.1:n.3+1223A>C
NM_005802.4:c.4-243A>C (TOPORS) NP_005793.2:n.4-243A>C
NR_033991.1:n.68T>G (SMIM27)
NM_001349118.1:c.-684T>G (SMIM27) NP_001336047.1:n.-684T>G
XM_024447368.1:c.205+13T>G (SMIM27) XP_024303136.1:n.205+13T>G
NM_005802.5:c.4-243A>C (TOPORS) MANE Select NP_005793.2:n.4-243A>C
NM_001195622.2:c.3+1223A>C (TOPORS) NP_001182551.1:n.3+1223A>C