Canonical Allele Identifier: CA412982314
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535077A>C (hg19) chrX:g.38675823A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675823A>C , CM000685.2:g.38675823A>C GRCh38
NC_000023.10:g.38535077A>C , CM000685.1:g.38535077A>C GRCh37
NC_000023.9:g.38420021A>C NCBI36
NG_009160.1:g.119347A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.560A>C MANE Select ENSP00000367743.2:p.His187Pro
ENST00000286824.6:c.611A>C ENSP00000286824.6:p.His204Pro
ENST00000378482.6:c.560A>C ENSP00000367743.2:p.His187Pro
ENST00000419600.3:n.504A>C
ENST00000465127.1:c.650A>C ENSP00000417050.1:p.His217Pro
ENST00000471410.5:c.*586A>C ENSP00000419290.1:n.*586A>C
ENST00000475216.5:c.*553A>C ENSP00000418586.1:n.*553A>C
NM_004615.3:c.560A>C NP_004606.2:p.His187Pro
NM_004615.4:c.560A>C MANE Select NP_004606.2:p.His187Pro
Search 100 bp 5'
Search 100 bp 3'