Canonical Allele Identifier: CA412982307
Gene: TSPAN7 HGNC NCBI

Linked Data

dbSNP Id: rs2069850056
MyVariant Identifiers: chrX:g.38535073C>A (hg19) chrX:g.38675819C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675819C>A , CM000685.2:g.38675819C>A GRCh38
NC_000023.10:g.38535073C>A , CM000685.1:g.38535073C>A GRCh37
NC_000023.9:g.38420017C>A NCBI36
NG_009160.1:g.119343C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.556C>A MANE Select ENSP00000367743.2:p.Leu186Ile
ENST00000286824.6:c.607C>A ENSP00000286824.6:p.Leu203Ile
ENST00000378482.6:c.556C>A ENSP00000367743.2:p.Leu186Ile
ENST00000419600.3:n.500C>A
ENST00000465127.1:c.646C>A ENSP00000417050.1:p.Leu216Ile
ENST00000471410.5:c.*582C>A ENSP00000419290.1:n.*582C>A
ENST00000475216.5:c.*549C>A ENSP00000418586.1:n.*549C>A
NM_004615.3:c.556C>A NP_004606.2:p.Leu186Ile
NM_004615.4:c.556C>A MANE Select NP_004606.2:p.Leu186Ile
Search 100 bp 5'
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