Canonical Allele Identifier: CA412982329
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535083T>A (hg19) chrX:g.38675829T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675829T>A , CM000685.2:g.38675829T>A GRCh38
NC_000023.10:g.38535083T>A , CM000685.1:g.38535083T>A GRCh37
NC_000023.9:g.38420027T>A NCBI36
NG_009160.1:g.119353T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.566T>A MANE Select ENSP00000367743.2:p.Leu189Gln
ENST00000286824.6:c.617T>A ENSP00000286824.6:p.Leu206Gln
ENST00000378482.6:c.566T>A ENSP00000367743.2:p.Leu189Gln
ENST00000419600.3:n.510T>A
ENST00000465127.1:c.656T>A ENSP00000417050.1:p.Leu219Gln
ENST00000471410.5:c.*592T>A ENSP00000419290.1:n.*592T>A
ENST00000475216.5:c.*559T>A ENSP00000418586.1:n.*559T>A
NM_004615.3:c.566T>A NP_004606.2:p.Leu189Gln
NM_004615.4:c.566T>A MANE Select NP_004606.2:p.Leu189Gln
Search 100 bp 5'
Search 100 bp 3'