Canonical Allele Identifier: CA2424970096
Gene: TSPAN7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675926A= , CM000685.2:g.38675926A= GRCh38
NC_000023.10:g.38535180A= , CM000685.1:g.38535180A= GRCh37
NC_000023.9:g.38420124A= NCBI36
NG_009160.1:g.119450A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+66A= MANE Select ENSP00000367743.2:n.597+66A=
ENST00000286824.6:c.648+66A= ENSP00000286824.6:n.648+66A=
ENST00000378482.6:c.597+66A= ENSP00000367743.2:n.597+66A=
ENST00000419600.3:n.541+66A=
ENST00000465127.1:c.687+66A= ENSP00000417050.1:n.687+66A=
ENST00000471410.5:c.*623+66A= ENSP00000419290.1:n.*623+66A=
ENST00000475216.5:c.*590+66A= ENSP00000418586.1:n.*590+66A=
NM_004615.3:c.597+66A= NP_004606.2:n.597+66A=
NM_004615.4:c.597+66A= MANE Select NP_004606.2:n.597+66A=
Search 100 bp 5'
Search 100 bp 3'