Canonical Allele Identifier: CA2515264133
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675809_38675810insGAGACGGCGA , CM000685.2:g.38675809_38675810insGAGACGGCGA GRCh38
NC_000023.10:g.38535063_38535064insGAGACGGCGA , CM000685.1:g.38535063_38535064insGAGACGGCGA GRCh37
NC_000023.9:g.38420007_38420008insGAGACGGCGA NCBI36
NG_009160.1:g.119333_119334insGAGACGGCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.546_547insGAGACGGCGA MANE Select ENSP00000367743.2:p.Pro183GlufsTer18
ENST00000286824.6:c.597_598insGAGACGGCGA ENSP00000286824.6:p.Pro200GlufsTer18
ENST00000378482.6:c.546_547insGAGACGGCGA ENSP00000367743.2:p.Pro183GlufsTer18
ENST00000419600.3:n.490_491insGAGACGGCGA
ENST00000465127.1:c.636_637insGAGACGGCGA ENSP00000417050.1:p.Pro213GlufsTer18
ENST00000471410.5:c.*572_*573insGAGACGGCGA ENSP00000419290.1:n.*572_*573insGAGACGGCGA
ENST00000475216.5:c.*539_*540insGAGACGGCGA ENSP00000418586.1:n.*539_*540insGAGACGGCGA
ENST00000488893.5:n.729_730insGAGACGGCGA
NM_004615.3:c.546_547insGAGACGGCGA NP_004606.2:p.Pro183GlufsTer18
NM_004615.4:c.546_547insGAGACGGCGA MANE Select NP_004606.2:p.Pro183GlufsTer18