Canonical Allele Identifier: CA10386125

Gene: TSPAN7

Linked Data

• dbSNP Id: rs776814898
• ExAC: X:38535065 C / T
• gnomAD v2: X-38535065-C-T
• MyVariant Identifiers: chrX:g.38535065C>T (hg19) ; chrX:g.38675811C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675811C>T , CM000685.2:g.38675811C>T	GRCh38
NC_000023.10:g.38535065C>T , CM000685.1:g.38535065C>T	GRCh37
NC_000023.9:g.38420009C>T	NCBI36
NG_009160.1:g.119335C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.548C>T MANE Select	ENSP00000367743.2:p.Pro183Leu
ENST00000286824.6:c.599C>T	ENSP00000286824.6:p.Pro200Leu
ENST00000378482.6:c.548C>T	ENSP00000367743.2:p.Pro183Leu
ENST00000419600.3:n.492C>T
ENST00000465127.1:c.638C>T	ENSP00000417050.1:p.Pro213Leu
ENST00000471410.5:c.*574C>T	ENSP00000419290.1:n.*574C>T
ENST00000475216.5:c.*541C>T	ENSP00000418586.1:n.*541C>T
ENST00000488893.5:n.731C>T
NM_004615.3:c.548C>T	NP_004606.2:p.Pro183Leu
NM_004615.4:c.548C>T MANE Select	NP_004606.2:p.Pro183Leu