Canonical Allele Identifier: CA412982139
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675745C>A , CM000685.2:g.38675745C>A GRCh38
NC_000023.10:g.38534999C>A , CM000685.1:g.38534999C>A GRCh37
NC_000023.9:g.38419943C>A NCBI36
NG_009160.1:g.119269C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.482C>A MANE Select ENSP00000367743.2:p.Thr161Asn
ENST00000286824.6:c.533C>A ENSP00000286824.6:p.Thr178Asn
ENST00000378482.6:c.482C>A ENSP00000367743.2:p.Thr161Asn
ENST00000419600.3:n.426C>A
ENST00000465127.1:c.572C>A ENSP00000417050.1:p.Thr191Asn
ENST00000471410.5:c.*508C>A ENSP00000419290.1:n.*508C>A
ENST00000475216.5:c.*475C>A ENSP00000418586.1:n.*475C>A
ENST00000488893.5:n.665C>A
NM_004615.3:c.482C>A NP_004606.2:p.Thr161Asn
NM_004615.4:c.482C>A MANE Select NP_004606.2:p.Thr161Asn