Canonical Allele Identifier: CA412982288

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535064C>A (hg19) ; chrX:g.38675810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675810C>A , CM000685.2:g.38675810C>A	GRCh38
NC_000023.10:g.38535064C>A , CM000685.1:g.38535064C>A	GRCh37
NC_000023.9:g.38420008C>A	NCBI36
NG_009160.1:g.119334C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.547C>A MANE Select	ENSP00000367743.2:p.Pro183Thr
ENST00000286824.6:c.598C>A	ENSP00000286824.6:p.Pro200Thr
ENST00000378482.6:c.547C>A	ENSP00000367743.2:p.Pro183Thr
ENST00000419600.3:n.491C>A
ENST00000465127.1:c.637C>A	ENSP00000417050.1:p.Pro213Thr
ENST00000471410.5:c.*573C>A	ENSP00000419290.1:n.*573C>A
ENST00000475216.5:c.*540C>A	ENSP00000418586.1:n.*540C>A
ENST00000488893.5:n.730C>A
NM_004615.3:c.547C>A	NP_004606.2:p.Pro183Thr
NM_004615.4:c.547C>A MANE Select	NP_004606.2:p.Pro183Thr