Canonical Allele Identifier: CA412982278

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535060T>A (hg19) ; chrX:g.38675806T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675806T>A , CM000685.2:g.38675806T>A	GRCh38
NC_000023.10:g.38535060T>A , CM000685.1:g.38535060T>A	GRCh37
NC_000023.9:g.38420004T>A	NCBI36
NG_009160.1:g.119330T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.543T>A MANE Select	ENSP00000367743.2:p.Cys181Ter
ENST00000286824.6:c.594T>A	ENSP00000286824.6:p.Cys198Ter
ENST00000378482.6:c.543T>A	ENSP00000367743.2:p.Cys181Ter
ENST00000419600.3:n.487T>A
ENST00000465127.1:c.633T>A	ENSP00000417050.1:p.Cys211Ter
ENST00000471410.5:c.*569T>A	ENSP00000419290.1:n.*569T>A
ENST00000475216.5:c.*536T>A	ENSP00000418586.1:n.*536T>A
ENST00000488893.5:n.726T>A
NM_004615.3:c.543T>A	NP_004606.2:p.Cys181Ter
NM_004615.4:c.543T>A MANE Select	NP_004606.2:p.Cys181Ter