Canonical Allele Identifier: CA2424970061
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675811C= , CM000685.2:g.38675811C= GRCh38
NC_000023.10:g.38535065C= , CM000685.1:g.38535065C= GRCh37
NC_000023.9:g.38420009C= NCBI36
NG_009160.1:g.119335C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.548C= MANE Select ENSP00000367743.2:p.Pro183=
ENST00000286824.6:c.599C= ENSP00000286824.6:p.Pro200=
ENST00000378482.6:c.548C= ENSP00000367743.2:p.Pro183=
ENST00000419600.3:n.492C=
ENST00000465127.1:c.638C= ENSP00000417050.1:p.Pro213=
ENST00000471410.5:c.*574C= ENSP00000419290.1:n.*574C=
ENST00000475216.5:c.*541C= ENSP00000418586.1:n.*541C=
ENST00000488893.5:n.731C=
NM_004615.3:c.548C= NP_004606.2:p.Pro183=
NM_004615.4:c.548C= MANE Select NP_004606.2:p.Pro183=