Canonical Allele Identifier: CA2424970044
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675772T= , CM000685.2:g.38675772T= GRCh38
NC_000023.10:g.38535026T= , CM000685.1:g.38535026T= GRCh37
NC_000023.9:g.38419970T= NCBI36
NG_009160.1:g.119296T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.509T= MANE Select ENSP00000367743.2:p.Ile170=
ENST00000286824.6:c.560T= ENSP00000286824.6:p.Ile187=
ENST00000378482.6:c.509T= ENSP00000367743.2:p.Ile170=
ENST00000419600.3:n.453T=
ENST00000465127.1:c.599T= ENSP00000417050.1:p.Ile200=
ENST00000471410.5:c.*535T= ENSP00000419290.1:n.*535T=
ENST00000475216.5:c.*502T= ENSP00000418586.1:n.*502T=
ENST00000488893.5:n.692T=
NM_004615.3:c.509T= NP_004606.2:p.Ile170=
NM_004615.4:c.509T= MANE Select NP_004606.2:p.Ile170=