Canonical Allele Identifier: CA412982318
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535078C>G (hg19) chrX:g.38675824C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675824C>G , CM000685.2:g.38675824C>G GRCh38
NC_000023.10:g.38535078C>G , CM000685.1:g.38535078C>G GRCh37
NC_000023.9:g.38420022C>G NCBI36
NG_009160.1:g.119348C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.561C>G MANE Select ENSP00000367743.2:p.His187Gln
ENST00000286824.6:c.612C>G ENSP00000286824.6:p.His204Gln
ENST00000378482.6:c.561C>G ENSP00000367743.2:p.His187Gln
ENST00000419600.3:n.505C>G
ENST00000465127.1:c.651C>G ENSP00000417050.1:p.His217Gln
ENST00000471410.5:c.*587C>G ENSP00000419290.1:n.*587C>G
ENST00000475216.5:c.*554C>G ENSP00000418586.1:n.*554C>G
NM_004615.3:c.561C>G NP_004606.2:p.His187Gln
NM_004615.4:c.561C>G MANE Select NP_004606.2:p.His187Gln
Search 100 bp 5'
Search 100 bp 3'