Canonical Allele Identifier: CA2693446498
Gene: TSPAN7 HGNC NCBI

Linked Data

gnomAD v4: X-38675606-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675610del , CM000685.2:g.38675610del GRCh38
NC_000023.10:g.38534864del , CM000685.1:g.38534864del GRCh37
NC_000023.9:g.38419808del NCBI36
NG_009160.1:g.119134del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-95del MANE Select ENSP00000367743.2:n.442-95del
ENST00000286824.6:c.493-95del ENSP00000286824.6:n.493-95del
ENST00000378482.6:c.442-95del ENSP00000367743.2:n.442-95del
ENST00000419600.3:n.386-95del
ENST00000465127.1:c.532-95del ENSP00000417050.1:n.532-95del
ENST00000471410.5:c.*468-95del ENSP00000419290.1:n.*468-95del
ENST00000475216.5:c.*435-95del ENSP00000418586.1:n.*435-95del
ENST00000488893.5:n.625-95del
NM_004615.3:c.442-95del NP_004606.2:n.442-95del
NM_004615.4:c.442-95del MANE Select NP_004606.2:n.442-95del
Search 100 bp 5'
Search 100 bp 3'