Canonical Allele Identifier: CA2424970116
Gene: TSPAN7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675987T= , CM000685.2:g.38675987T= GRCh38
NC_000023.10:g.38535241T= , CM000685.1:g.38535241T= GRCh37
NC_000023.9:g.38420185T= NCBI36
NG_009160.1:g.119511T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+127T= MANE Select ENSP00000367743.2:n.597+127T=
ENST00000286824.6:c.648+127T= ENSP00000286824.6:n.648+127T=
ENST00000378482.6:c.597+127T= ENSP00000367743.2:n.597+127T=
ENST00000419600.3:n.541+127T=
ENST00000465127.1:c.687+127T= ENSP00000417050.1:n.687+127T=
ENST00000471410.5:c.*623+127T= ENSP00000419290.1:n.*623+127T=
ENST00000475216.5:c.*590+127T= ENSP00000418586.1:n.*590+127T=
NM_004615.3:c.597+127T= NP_004606.2:n.597+127T=
NM_004615.4:c.597+127T= MANE Select NP_004606.2:n.597+127T=
Search 100 bp 5'
Search 100 bp 3'