Canonical Allele Identifier: CA10386137
Gene: TSPAN7 HGNC NCBI

Linked Data

dbSNP Id: rs767128840
ExAC: X:38535159 T / TG
gnomAD v2: X-38535159-T-TG
gnomAD v3: X-38675905-T-TG
gnomAD v4: X-38675905-T-TG
MyVariant Identifiers: chrX:g.38535160_38535161insG (hg19) chrX:g.38535159_38535160insG (hg19) chrX:g.38675905_38675906insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675912dup , CM000685.2:g.38675912dup GRCh38
NC_000023.10:g.38535166dup , CM000685.1:g.38535166dup GRCh37
NC_000023.9:g.38420110dup NCBI36
NG_009160.1:g.119436dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+52dup MANE Select ENSP00000367743.2:n.597+52dup
ENST00000286824.6:c.648+52dup ENSP00000286824.6:n.648+52dup
ENST00000378482.6:c.597+52dup ENSP00000367743.2:n.597+52dup
ENST00000419600.3:n.541+52dup
ENST00000465127.1:c.687+52dup ENSP00000417050.1:n.687+52dup
ENST00000471410.5:c.*623+52dup ENSP00000419290.1:n.*623+52dup
ENST00000475216.5:c.*590+52dup ENSP00000418586.1:n.*590+52dup
NM_004615.3:c.597+52dup NP_004606.2:n.597+52dup
NM_004615.4:c.597+52dup MANE Select NP_004606.2:n.597+52dup
Search 100 bp 5'
Search 100 bp 3'