Canonical Allele Identifier: CA515685535
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535105T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675851T>A , CM000685.2:g.38675851T>A GRCh38
NC_000023.10:g.38535105T>A , CM000685.1:g.38535105T>A GRCh37
NC_000023.9:g.38420049T>A NCBI36
NG_009160.1:g.119375T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.588T>A MANE Select ENSP00000367743.2:p.Val196=
ENST00000286824.6:c.639T>A ENSP00000286824.6:p.Val213=
ENST00000378482.6:c.588T>A ENSP00000367743.2:p.Val196=
ENST00000419600.3:n.532T>A
ENST00000465127.1:c.678T>A ENSP00000417050.1:p.Val226=
ENST00000471410.5:c.*614T>A ENSP00000419290.1:n.*614T>A
ENST00000475216.5:c.*581T>A ENSP00000418586.1:n.*581T>A
NM_004615.3:c.588T>A NP_004606.2:p.Val196=
NM_004615.4:c.588T>A MANE Select NP_004606.2:p.Val196=
Search 100 bp 5'
Search 100 bp 3'