Canonical Allele Identifier: CA412982177

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535016G>C (hg19) ; chrX:g.38675762G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675762G>C , CM000685.2:g.38675762G>C	GRCh38
NC_000023.10:g.38535016G>C , CM000685.1:g.38535016G>C	GRCh37
NC_000023.9:g.38419960G>C	NCBI36
NG_009160.1:g.119286G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.499G>C MANE Select	ENSP00000367743.2:p.Glu167Gln
ENST00000286824.6:c.550G>C	ENSP00000286824.6:p.Glu184Gln
ENST00000378482.6:c.499G>C	ENSP00000367743.2:p.Glu167Gln
ENST00000419600.3:n.443G>C
ENST00000465127.1:c.589G>C	ENSP00000417050.1:p.Glu197Gln
ENST00000471410.5:c.*525G>C	ENSP00000419290.1:n.*525G>C
ENST00000475216.5:c.*492G>C	ENSP00000418586.1:n.*492G>C
ENST00000488893.5:n.682G>C
NM_004615.3:c.499G>C	NP_004606.2:p.Glu167Gln
NM_004615.4:c.499G>C MANE Select	NP_004606.2:p.Glu167Gln