Canonical Allele Identifier: CA412982310

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535074T>A (hg19) ; chrX:g.38675820T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675820T>A , CM000685.2:g.38675820T>A	GRCh38
NC_000023.10:g.38535074T>A , CM000685.1:g.38535074T>A	GRCh37
NC_000023.9:g.38420018T>A	NCBI36
NG_009160.1:g.119344T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.557T>A MANE Select	ENSP00000367743.2:p.Leu186Gln
ENST00000286824.6:c.608T>A	ENSP00000286824.6:p.Leu203Gln
ENST00000378482.6:c.557T>A	ENSP00000367743.2:p.Leu186Gln
ENST00000419600.3:n.501T>A
ENST00000465127.1:c.647T>A	ENSP00000417050.1:p.Leu216Gln
ENST00000471410.5:c.*583T>A	ENSP00000419290.1:n.*583T>A
ENST00000475216.5:c.*550T>A	ENSP00000418586.1:n.*550T>A
NM_004615.3:c.557T>A	NP_004606.2:p.Leu186Gln
NM_004615.4:c.557T>A MANE Select	NP_004606.2:p.Leu186Gln