Canonical Allele Identifier: CA412982139

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38534999C>A (hg19) ; chrX:g.38675745C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675745C>A , CM000685.2:g.38675745C>A	GRCh38
NC_000023.10:g.38534999C>A , CM000685.1:g.38534999C>A	GRCh37
NC_000023.9:g.38419943C>A	NCBI36
NG_009160.1:g.119269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.482C>A MANE Select	ENSP00000367743.2:p.Thr161Asn
ENST00000286824.6:c.533C>A	ENSP00000286824.6:p.Thr178Asn
ENST00000378482.6:c.482C>A	ENSP00000367743.2:p.Thr161Asn
ENST00000419600.3:n.426C>A
ENST00000465127.1:c.572C>A	ENSP00000417050.1:p.Thr191Asn
ENST00000471410.5:c.*508C>A	ENSP00000419290.1:n.*508C>A
ENST00000475216.5:c.*475C>A	ENSP00000418586.1:n.*475C>A
ENST00000488893.5:n.665C>A
NM_004615.3:c.482C>A	NP_004606.2:p.Thr161Asn
NM_004615.4:c.482C>A MANE Select	NP_004606.2:p.Thr161Asn