Canonical Allele Identifier: CA412982166

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535010T>G (hg19) ; chrX:g.38675756T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675756T>G , CM000685.2:g.38675756T>G	GRCh38
NC_000023.10:g.38535010T>G , CM000685.1:g.38535010T>G	GRCh37
NC_000023.9:g.38419954T>G	NCBI36
NG_009160.1:g.119280T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.493T>G MANE Select	ENSP00000367743.2:p.Phe165Val
ENST00000286824.6:c.544T>G	ENSP00000286824.6:p.Phe182Val
ENST00000378482.6:c.493T>G	ENSP00000367743.2:p.Phe165Val
ENST00000419600.3:n.437T>G
ENST00000465127.1:c.583T>G	ENSP00000417050.1:p.Phe195Val
ENST00000471410.5:c.*519T>G	ENSP00000419290.1:n.*519T>G
ENST00000475216.5:c.*486T>G	ENSP00000418586.1:n.*486T>G
ENST00000488893.5:n.676T>G
NM_004615.3:c.493T>G	NP_004606.2:p.Phe165Val
NM_004615.4:c.493T>G MANE Select	NP_004606.2:p.Phe165Val