Canonical Allele Identifier: CA412982343

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535089T>A (hg19) ; chrX:g.38675835T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675835T>A , CM000685.2:g.38675835T>A	GRCh38
NC_000023.10:g.38535089T>A , CM000685.1:g.38535089T>A	GRCh37
NC_000023.9:g.38420033T>A	NCBI36
NG_009160.1:g.119359T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.572T>A MANE Select	ENSP00000367743.2:p.Val191Glu
ENST00000286824.6:c.623T>A	ENSP00000286824.6:p.Val208Glu
ENST00000378482.6:c.572T>A	ENSP00000367743.2:p.Val191Glu
ENST00000419600.3:n.516T>A
ENST00000465127.1:c.662T>A	ENSP00000417050.1:p.Val221Glu
ENST00000471410.5:c.*598T>A	ENSP00000419290.1:n.*598T>A
ENST00000475216.5:c.*565T>A	ENSP00000418586.1:n.*565T>A
NM_004615.3:c.572T>A	NP_004606.2:p.Val191Glu
NM_004615.4:c.572T>A MANE Select	NP_004606.2:p.Val191Glu