Canonical Allele Identifier: CA412982048

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38534963G>A (hg19) ; chrX:g.38675709G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675709G>A , CM000685.2:g.38675709G>A	GRCh38
NC_000023.10:g.38534963G>A , CM000685.1:g.38534963G>A	GRCh37
NC_000023.9:g.38419907G>A	NCBI36
NG_009160.1:g.119233G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378482.7:c.446G>A MANE Select	ENSP00000367743.2:p.Ser149Asn
ENST00000286824.6:c.497G>A	ENSP00000286824.6:p.Ser166Asn
ENST00000378482.6:c.446G>A	ENSP00000367743.2:p.Ser149Asn
ENST00000419600.3:n.390G>A
ENST00000465127.1:c.536G>A	ENSP00000417050.1:p.Ser179Asn
ENST00000471410.5:c.*472G>A	ENSP00000419290.1:n.*472G>A
ENST00000475216.5:c.*439G>A	ENSP00000418586.1:n.*439G>A
ENST00000488893.5:n.629G>A
NM_004615.3:c.446G>A	NP_004606.2:p.Ser149Asn
NM_004615.4:c.446G>A MANE Select	NP_004606.2:p.Ser149Asn