Canonical Allele Identifier: CA515685509
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535090G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675836G>A , CM000685.2:g.38675836G>A GRCh38
NC_000023.10:g.38535090G>A , CM000685.1:g.38535090G>A GRCh37
NC_000023.9:g.38420034G>A NCBI36
NG_009160.1:g.119360G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.573G>A MANE Select ENSP00000367743.2:p.Val191=
ENST00000286824.6:c.624G>A ENSP00000286824.6:p.Val208=
ENST00000378482.6:c.573G>A ENSP00000367743.2:p.Val191=
ENST00000419600.3:n.517G>A
ENST00000465127.1:c.663G>A ENSP00000417050.1:p.Val221=
ENST00000471410.5:c.*599G>A ENSP00000419290.1:n.*599G>A
ENST00000475216.5:c.*566G>A ENSP00000418586.1:n.*566G>A
NM_004615.3:c.573G>A NP_004606.2:p.Val191=
NM_004615.4:c.573G>A MANE Select NP_004606.2:p.Val191=
Search 100 bp 5'
Search 100 bp 3'