Canonical Allele Identifier: CA515685498
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535087T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675833T>C , CM000685.2:g.38675833T>C GRCh38
NC_000023.10:g.38535087T>C , CM000685.1:g.38535087T>C GRCh37
NC_000023.9:g.38420031T>C NCBI36
NG_009160.1:g.119357T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.570T>C MANE Select ENSP00000367743.2:p.Thr190=
ENST00000286824.6:c.621T>C ENSP00000286824.6:p.Thr207=
ENST00000378482.6:c.570T>C ENSP00000367743.2:p.Thr190=
ENST00000419600.3:n.514T>C
ENST00000465127.1:c.660T>C ENSP00000417050.1:p.Thr220=
ENST00000471410.5:c.*596T>C ENSP00000419290.1:n.*596T>C
ENST00000475216.5:c.*563T>C ENSP00000418586.1:n.*563T>C
NM_004615.3:c.570T>C NP_004606.2:p.Thr190=
NM_004615.4:c.570T>C MANE Select NP_004606.2:p.Thr190=
Search 100 bp 5'
Search 100 bp 3'