Canonical Allele Identifier: CA875199928

Gene: TSPAN7

Linked Data

• dbSNP Id: rs1215746078
• gnomAD v3: X-38675693-C-G
• gnomAD v4: X-38675693-C-G
• MyVariant Identifiers: chrX:g.38534947C>G (hg19) ; chrX:g.38675693C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675693C>G , CM000685.2:g.38675693C>G	GRCh38
NC_000023.10:g.38534947C>G , CM000685.1:g.38534947C>G	GRCh37
NC_000023.9:g.38419891C>G	NCBI36
NG_009160.1:g.119217C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-12C>G MANE Select	ENSP00000367743.2:n.442-12C>G
ENST00000286824.6:c.493-12C>G	ENSP00000286824.6:n.493-12C>G
ENST00000378482.6:c.442-12C>G	ENSP00000367743.2:n.442-12C>G
ENST00000419600.3:n.386-12C>G
ENST00000465127.1:c.532-12C>G	ENSP00000417050.1:n.532-12C>G
ENST00000471410.5:c.*468-12C>G	ENSP00000419290.1:n.*468-12C>G
ENST00000475216.5:c.*435-12C>G	ENSP00000418586.1:n.*435-12C>G
ENST00000488893.5:n.625-12C>G
NM_004615.3:c.442-12C>G	NP_004606.2:n.442-12C>G
NM_004615.4:c.442-12C>G MANE Select	NP_004606.2:n.442-12C>G