Canonical Allele Identifier: CA1132427503
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675811_38675812insGA , CM000685.2:g.38675811_38675812insGA GRCh38
NC_000023.10:g.38535065_38535066insGA , CM000685.1:g.38535065_38535066insGA GRCh37
NC_000023.9:g.38420009_38420010insGA NCBI36
NG_009160.1:g.119335_119336insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.548_549insGA MANE Select ENSP00000367743.2:p.Gln184ThrfsTer7
ENST00000286824.6:c.599_600insGA ENSP00000286824.6:p.Gln201ThrfsTer7
ENST00000378482.6:c.548_549insGA ENSP00000367743.2:p.Gln184ThrfsTer7
ENST00000419600.3:n.492_493insGA
ENST00000465127.1:c.638_639insGA ENSP00000417050.1:p.Gln214ThrfsTer7
ENST00000471410.5:c.*574_*575insGA ENSP00000419290.1:n.*574_*575insGA
ENST00000475216.5:c.*541_*542insGA ENSP00000418586.1:n.*541_*542insGA
ENST00000488893.5:n.731_732insGA
NM_004615.3:c.548_549insGA NP_004606.2:p.Gln184ThrfsTer7
NM_004615.4:c.548_549insGA MANE Select NP_004606.2:p.Gln184ThrfsTer7