Canonical Allele Identifier: CA412982174

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535014T>C (hg19) ; chrX:g.38675760T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675760T>C , CM000685.2:g.38675760T>C	GRCh38
NC_000023.10:g.38535014T>C , CM000685.1:g.38535014T>C	GRCh37
NC_000023.9:g.38419958T>C	NCBI36
NG_009160.1:g.119284T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.497T>C MANE Select	ENSP00000367743.2:p.Leu166Pro
ENST00000286824.6:c.548T>C	ENSP00000286824.6:p.Leu183Pro
ENST00000378482.6:c.497T>C	ENSP00000367743.2:p.Leu166Pro
ENST00000419600.3:n.441T>C
ENST00000465127.1:c.587T>C	ENSP00000417050.1:p.Leu196Pro
ENST00000471410.5:c.*523T>C	ENSP00000419290.1:n.*523T>C
ENST00000475216.5:c.*490T>C	ENSP00000418586.1:n.*490T>C
ENST00000488893.5:n.680T>C
NM_004615.3:c.497T>C	NP_004606.2:p.Leu166Pro
NM_004615.4:c.497T>C MANE Select	NP_004606.2:p.Leu166Pro