Canonical Allele Identifier: CA412982316

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535077A>T (hg19) ; chrX:g.38675823A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675823A>T , CM000685.2:g.38675823A>T	GRCh38
NC_000023.10:g.38535077A>T , CM000685.1:g.38535077A>T	GRCh37
NC_000023.9:g.38420021A>T	NCBI36
NG_009160.1:g.119347A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.560A>T MANE Select	ENSP00000367743.2:p.His187Leu
ENST00000286824.6:c.611A>T	ENSP00000286824.6:p.His204Leu
ENST00000378482.6:c.560A>T	ENSP00000367743.2:p.His187Leu
ENST00000419600.3:n.504A>T
ENST00000465127.1:c.650A>T	ENSP00000417050.1:p.His217Leu
ENST00000471410.5:c.*586A>T	ENSP00000419290.1:n.*586A>T
ENST00000475216.5:c.*553A>T	ENSP00000418586.1:n.*553A>T
NM_004615.3:c.560A>T	NP_004606.2:p.His187Leu
NM_004615.4:c.560A>T MANE Select	NP_004606.2:p.His187Leu