Canonical Allele Identifier: CA875199907

Gene: TSPAN7

Linked Data

• dbSNP Id: rs1418882295
• MyVariant Identifiers: chrX:g.38534829A>G (hg19) ; chrX:g.38675575A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675575A>G , CM000685.2:g.38675575A>G	GRCh38
NC_000023.10:g.38534829A>G , CM000685.1:g.38534829A>G	GRCh37
NC_000023.9:g.38419773A>G	NCBI36
NG_009160.1:g.119099A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-130A>G MANE Select	ENSP00000367743.2:n.442-130A>G
ENST00000286824.6:c.493-130A>G	ENSP00000286824.6:n.493-130A>G
ENST00000378482.6:c.442-130A>G	ENSP00000367743.2:n.442-130A>G
ENST00000419600.3:n.386-130A>G
ENST00000465127.1:c.532-130A>G	ENSP00000417050.1:n.532-130A>G
ENST00000471410.5:c.*468-130A>G	ENSP00000419290.1:n.*468-130A>G
ENST00000475216.5:c.*435-130A>G	ENSP00000418586.1:n.*435-130A>G
ENST00000488893.5:n.625-130A>G
NM_004615.3:c.442-130A>G	NP_004606.2:n.442-130A>G
NM_004615.4:c.442-130A>G MANE Select	NP_004606.2:n.442-130A>G