Canonical Allele Identifier: CA875200407

Gene: TSPAN7

Linked Data

• dbSNP Id: rs1221290923
• MyVariant Identifiers: chrX:g.38535153A>G (hg19) ; chrX:g.38675899A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675899A>G , CM000685.2:g.38675899A>G	GRCh38
NC_000023.10:g.38535153A>G , CM000685.1:g.38535153A>G	GRCh37
NC_000023.9:g.38420097A>G	NCBI36
NG_009160.1:g.119423A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+39A>G MANE Select	ENSP00000367743.2:n.597+39A>G
ENST00000286824.6:c.648+39A>G	ENSP00000286824.6:n.648+39A>G
ENST00000378482.6:c.597+39A>G	ENSP00000367743.2:n.597+39A>G
ENST00000419600.3:n.541+39A>G
ENST00000465127.1:c.687+39A>G	ENSP00000417050.1:n.687+39A>G
ENST00000471410.5:c.*623+39A>G	ENSP00000419290.1:n.*623+39A>G
ENST00000475216.5:c.*590+39A>G	ENSP00000418586.1:n.*590+39A>G
NM_004615.3:c.597+39A>G	NP_004606.2:n.597+39A>G
NM_004615.4:c.597+39A>G MANE Select	NP_004606.2:n.597+39A>G