Canonical Allele Identifier: CA412982357
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675843A>G , CM000685.2:g.38675843A>G GRCh38
NC_000023.10:g.38535097A>G , CM000685.1:g.38535097A>G GRCh37
NC_000023.9:g.38420041A>G NCBI36
NG_009160.1:g.119367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.580A>G MANE Select ENSP00000367743.2:p.Thr194Ala
ENST00000286824.6:c.631A>G ENSP00000286824.6:p.Thr211Ala
ENST00000378482.6:c.580A>G ENSP00000367743.2:p.Thr194Ala
ENST00000419600.3:n.524A>G
ENST00000465127.1:c.670A>G ENSP00000417050.1:p.Thr224Ala
ENST00000471410.5:c.*606A>G ENSP00000419290.1:n.*606A>G
ENST00000475216.5:c.*573A>G ENSP00000418586.1:n.*573A>G
NM_004615.3:c.580A>G NP_004606.2:p.Thr194Ala
NM_004615.4:c.580A>G MANE Select NP_004606.2:p.Thr194Ala