Canonical Allele Identifier: CA2783454054
Gene: TOPORS HGNC NCBI
SMIM27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32551140_32551141insAGT , CM000671.2:g.32551140_32551141insAGT GRCh38
NC_000009.11:g.32551138_32551139insAGT , CM000671.1:g.32551138_32551139insAGT GRCh37
NC_000009.10:g.32541138_32541139insAGT NCBI36
NG_017050.1:g.6484_6485insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.4-173_4-172insACT (TOPORS) MANE Select ENSP00000353735.2:n.4-173_4-172insACT
ENST00000680198.1:c.4-173_4-172insACT ENSP00000505143.1:n.4-173_4-172insACT
ENST00000681750.1:c.-239-173_-239-172insACT ENSP00000506413.1:n.-239-173_-239-172insACT
ENST00000360538.6:c.4-173_4-172insACT (TOPORS) ENSP00000353735.2:n.4-173_4-172insACT
ENST00000379858.1:c.3+1293_3+1294insACT (TOPORS) ENSP00000369187.1:n.3+1293_3+1294insACT
NM_001195622.1:c.3+1293_3+1294insACT (TOPORS) NP_001182551.1:n.3+1293_3+1294insACT
NM_005802.4:c.4-173_4-172insACT (TOPORS) NP_005793.2:n.4-173_4-172insACT
XM_024447368.1:c.147_148insAGT (SMIM27) XP_024303136.1:p.Pro49_Ser50insSer
NM_005802.5:c.4-173_4-172insACT (TOPORS) MANE Select NP_005793.2:n.4-173_4-172insACT
NM_001195622.2:c.3+1293_3+1294insACT (TOPORS) NP_001182551.1:n.3+1293_3+1294insACT