Canonical Allele Identifier: CA515685531
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535099C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675845C>A , CM000685.2:g.38675845C>A GRCh38
NC_000023.10:g.38535099C>A , CM000685.1:g.38535099C>A GRCh37
NC_000023.9:g.38420043C>A NCBI36
NG_009160.1:g.119369C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.582C>A MANE Select ENSP00000367743.2:p.Thr194=
ENST00000286824.6:c.633C>A ENSP00000286824.6:p.Thr211=
ENST00000378482.6:c.582C>A ENSP00000367743.2:p.Thr194=
ENST00000419600.3:n.526C>A
ENST00000465127.1:c.672C>A ENSP00000417050.1:p.Thr224=
ENST00000471410.5:c.*608C>A ENSP00000419290.1:n.*608C>A
ENST00000475216.5:c.*575C>A ENSP00000418586.1:n.*575C>A
NM_004615.3:c.582C>A NP_004606.2:p.Thr194=
NM_004615.4:c.582C>A MANE Select NP_004606.2:p.Thr194=
Search 100 bp 5'
Search 100 bp 3'