Canonical Allele Identifier: CA2424970103
Gene: TSPAN7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675953T= , CM000685.2:g.38675953T= GRCh38
NC_000023.10:g.38535207T= , CM000685.1:g.38535207T= GRCh37
NC_000023.9:g.38420151T= NCBI36
NG_009160.1:g.119477T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+93T= MANE Select ENSP00000367743.2:n.597+93T=
ENST00000286824.6:c.648+93T= ENSP00000286824.6:n.648+93T=
ENST00000378482.6:c.597+93T= ENSP00000367743.2:n.597+93T=
ENST00000419600.3:n.541+93T=
ENST00000465127.1:c.687+93T= ENSP00000417050.1:n.687+93T=
ENST00000471410.5:c.*623+93T= ENSP00000419290.1:n.*623+93T=
ENST00000475216.5:c.*590+93T= ENSP00000418586.1:n.*590+93T=
NM_004615.3:c.597+93T= NP_004606.2:n.597+93T=
NM_004615.4:c.597+93T= MANE Select NP_004606.2:n.597+93T=
Search 100 bp 5'
Search 100 bp 3'