Canonical Allele Identifier: CA412982382
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675854C>G , CM000685.2:g.38675854C>G GRCh38
NC_000023.10:g.38535108C>G , CM000685.1:g.38535108C>G GRCh37
NC_000023.9:g.38420052C>G NCBI36
NG_009160.1:g.119378C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.591C>G MANE Select ENSP00000367743.2:p.Asn197Lys
ENST00000286824.6:c.642C>G ENSP00000286824.6:p.Asn214Lys
ENST00000378482.6:c.591C>G ENSP00000367743.2:p.Asn197Lys
ENST00000419600.3:n.535C>G
ENST00000465127.1:c.681C>G ENSP00000417050.1:p.Asn227Lys
ENST00000471410.5:c.*617C>G ENSP00000419290.1:n.*617C>G
ENST00000475216.5:c.*584C>G ENSP00000418586.1:n.*584C>G
NM_004615.3:c.591C>G NP_004606.2:p.Asn197Lys
NM_004615.4:c.591C>G MANE Select NP_004606.2:p.Asn197Lys