Canonical Allele Identifier: CA15005765

Gene: TSPAN7

Linked Data

• dbSNP Id: rs4826996
• gnomAD v2: X-38535174-A-G
• gnomAD v3: X-38675920-A-G
• gnomAD v4: X-38675920-A-G
• MyVariant Identifiers: chrX:g.38535174A>G (hg19) ; chrX:g.38675920A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675920A>G , CM000685.2:g.38675920A>G	GRCh38
NC_000023.10:g.38535174A>G , CM000685.1:g.38535174A>G	GRCh37
NC_000023.9:g.38420118A>G	NCBI36
NG_009160.1:g.119444A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+60A>G MANE Select	ENSP00000367743.2:n.597+60A>G
ENST00000286824.6:c.648+60A>G	ENSP00000286824.6:n.648+60A>G
ENST00000378482.6:c.597+60A>G	ENSP00000367743.2:n.597+60A>G
ENST00000419600.3:n.541+60A>G
ENST00000465127.1:c.687+60A>G	ENSP00000417050.1:n.687+60A>G
ENST00000471410.5:c.*623+60A>G	ENSP00000419290.1:n.*623+60A>G
ENST00000475216.5:c.*590+60A>G	ENSP00000418586.1:n.*590+60A>G
NM_004615.3:c.597+60A>G	NP_004606.2:n.597+60A>G
NM_004615.4:c.597+60A>G MANE Select	NP_004606.2:n.597+60A>G