Canonical Allele Identifier: CA412982387

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535110A>T (hg19) ; chrX:g.38675856A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675856A>T , CM000685.2:g.38675856A>T	GRCh38
NC_000023.10:g.38535110A>T , CM000685.1:g.38535110A>T	GRCh37
NC_000023.9:g.38420054A>T	NCBI36
NG_009160.1:g.119380A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.593A>T MANE Select	ENSP00000367743.2:p.Gln198Leu
ENST00000286824.6:c.644A>T	ENSP00000286824.6:p.Gln215Leu
ENST00000378482.6:c.593A>T	ENSP00000367743.2:p.Gln198Leu
ENST00000419600.3:n.537A>T
ENST00000465127.1:c.683A>T	ENSP00000417050.1:p.Gln228Leu
ENST00000471410.5:c.*619A>T	ENSP00000419290.1:n.*619A>T
ENST00000475216.5:c.*586A>T	ENSP00000418586.1:n.*586A>T
NM_004615.3:c.593A>T	NP_004606.2:p.Gln198Leu
NM_004615.4:c.593A>T MANE Select	NP_004606.2:p.Gln198Leu