Canonical Allele Identifier: CA412982332
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535085A>C (hg19) chrX:g.38675831A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675831A>C , CM000685.2:g.38675831A>C GRCh38
NC_000023.10:g.38535085A>C , CM000685.1:g.38535085A>C GRCh37
NC_000023.9:g.38420029A>C NCBI36
NG_009160.1:g.119355A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.568A>C MANE Select ENSP00000367743.2:p.Thr190Pro
ENST00000286824.6:c.619A>C ENSP00000286824.6:p.Thr207Pro
ENST00000378482.6:c.568A>C ENSP00000367743.2:p.Thr190Pro
ENST00000419600.3:n.512A>C
ENST00000465127.1:c.658A>C ENSP00000417050.1:p.Thr220Pro
ENST00000471410.5:c.*594A>C ENSP00000419290.1:n.*594A>C
ENST00000475216.5:c.*561A>C ENSP00000418586.1:n.*561A>C
NM_004615.3:c.568A>C NP_004606.2:p.Thr190Pro
NM_004615.4:c.568A>C MANE Select NP_004606.2:p.Thr190Pro
Search 100 bp 5'
Search 100 bp 3'