Canonical Allele Identifier: CA10386135
Gene: TSPAN7 HGNC NCBI

Linked Data

dbSNP Id: rs755630257
ExAC: X:38535142 G / A
gnomAD v2: X-38535142-G-A
gnomAD v3: X-38675888-G-A
gnomAD v4: X-38675888-G-A
MyVariant Identifiers: chrX:g.38535142G>A (hg19) chrX:g.38675888G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675888G>A , CM000685.2:g.38675888G>A GRCh38
NC_000023.10:g.38535142G>A , CM000685.1:g.38535142G>A GRCh37
NC_000023.9:g.38420086G>A NCBI36
NG_009160.1:g.119412G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+28G>A MANE Select ENSP00000367743.2:n.597+28G>A
ENST00000286824.6:c.648+28G>A ENSP00000286824.6:n.648+28G>A
ENST00000378482.6:c.597+28G>A ENSP00000367743.2:n.597+28G>A
ENST00000419600.3:n.541+28G>A
ENST00000465127.1:c.687+28G>A ENSP00000417050.1:n.687+28G>A
ENST00000471410.5:c.*623+28G>A ENSP00000419290.1:n.*623+28G>A
ENST00000475216.5:c.*590+28G>A ENSP00000418586.1:n.*590+28G>A
NM_004615.3:c.597+28G>A NP_004606.2:n.597+28G>A
NM_004615.4:c.597+28G>A MANE Select NP_004606.2:n.597+28G>A
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