Canonical Allele Identifier: CA2540522316
Gene: TSPAN7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675810_38675811insTTA , CM000685.2:g.38675810_38675811insTTA GRCh38
NC_000023.10:g.38535064_38535065insTTA , CM000685.1:g.38535064_38535065insTTA GRCh37
NC_000023.9:g.38420008_38420009insTTA NCBI36
NG_009160.1:g.119334_119335insTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.547_548insTTA MANE Select ENSP00000367743.2:p.Pro183delinsLeuThr
ENST00000286824.6:c.598_599insTTA ENSP00000286824.6:p.Pro200delinsLeuThr
ENST00000378482.6:c.547_548insTTA ENSP00000367743.2:p.Pro183delinsLeuThr
ENST00000419600.3:n.491_492insTTA
ENST00000465127.1:c.637_638insTTA ENSP00000417050.1:p.Pro213delinsLeuThr
ENST00000471410.5:c.*573_*574insTTA ENSP00000419290.1:n.*573_*574insTTA
ENST00000475216.5:c.*540_*541insTTA ENSP00000418586.1:n.*540_*541insTTA
ENST00000488893.5:n.730_731insTTA
NM_004615.3:c.547_548insTTA NP_004606.2:p.Pro183delinsLeuThr
NM_004615.4:c.547_548insTTA MANE Select NP_004606.2:p.Pro183delinsLeuThr
Search 100 bp 5'
Search 100 bp 3'