Canonical Allele Identifier: CA2783454043
Gene: TOPORS HGNC NCBI
SMIM27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32551097_32551098insA , CM000671.2:g.32551097_32551098insA GRCh38
NC_000009.11:g.32551095_32551096insA , CM000671.1:g.32551095_32551096insA GRCh37
NC_000009.10:g.32541095_32541096insA NCBI36
NG_017050.1:g.6527_6528insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.4-130_4-129insT (TOPORS) MANE Select ENSP00000353735.2:n.4-130_4-129insT
ENST00000680198.1:c.4-130_4-129insT ENSP00000505143.1:n.4-130_4-129insT
ENST00000681750.1:c.-239-130_-239-129insT ENSP00000506413.1:n.-239-130_-239-129insT
ENST00000360538.6:c.4-130_4-129insT (TOPORS) ENSP00000353735.2:n.4-130_4-129insT
ENST00000379858.1:c.3+1336_3+1337insT (TOPORS) ENSP00000369187.1:n.3+1336_3+1337insT
NM_001195622.1:c.3+1336_3+1337insT (TOPORS) NP_001182551.1:n.3+1336_3+1337insT
NM_005802.4:c.4-130_4-129insT (TOPORS) NP_005793.2:n.4-130_4-129insT
XM_024447368.1:c.104_105insA (SMIM27) XP_024303136.1:p.Pro36AlafsTer?
NM_005802.5:c.4-130_4-129insT (TOPORS) MANE Select NP_005793.2:n.4-130_4-129insT
NM_001195622.2:c.3+1336_3+1337insT (TOPORS) NP_001182551.1:n.3+1336_3+1337insT