Canonical Allele Identifier: CA2424970086
Gene: TSPAN7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675908G= , CM000685.2:g.38675908G= GRCh38
NC_000023.10:g.38535162G= , CM000685.1:g.38535162G= GRCh37
NC_000023.9:g.38420106G= NCBI36
NG_009160.1:g.119432G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+48G= MANE Select ENSP00000367743.2:n.597+48G=
ENST00000286824.6:c.648+48G= ENSP00000286824.6:n.648+48G=
ENST00000378482.6:c.597+48G= ENSP00000367743.2:n.597+48G=
ENST00000419600.3:n.541+48G=
ENST00000465127.1:c.687+48G= ENSP00000417050.1:n.687+48G=
ENST00000471410.5:c.*623+48G= ENSP00000419290.1:n.*623+48G=
ENST00000475216.5:c.*590+48G= ENSP00000418586.1:n.*590+48G=
NM_004615.3:c.597+48G= NP_004606.2:n.597+48G=
NM_004615.4:c.597+48G= MANE Select NP_004606.2:n.597+48G=
Search 100 bp 5'
Search 100 bp 3'