Canonical Allele Identifier: CA412982041

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38534959C>G (hg19) ; chrX:g.38675705C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675705C>G , CM000685.2:g.38675705C>G	GRCh38
NC_000023.10:g.38534959C>G , CM000685.1:g.38534959C>G	GRCh37
NC_000023.9:g.38419903C>G	NCBI36
NG_009160.1:g.119229C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378482.7:c.442C>G MANE Select	ENSP00000367743.2:p.Leu148Val
ENST00000286824.6:c.493C>G	ENSP00000286824.6:p.Leu165Val
ENST00000378482.6:c.442C>G	ENSP00000367743.2:p.Leu148Val
ENST00000419600.3:n.386C>G
ENST00000465127.1:c.532C>G	ENSP00000417050.1:p.Leu178Val
ENST00000471410.5:c.*468C>G	ENSP00000419290.1:n.*468C>G
ENST00000475216.5:c.*435C>G	ENSP00000418586.1:n.*435C>G
ENST00000488893.5:n.625C>G
NM_004615.3:c.442C>G	NP_004606.2:p.Leu148Val
NM_004615.4:c.442C>G MANE Select	NP_004606.2:p.Leu148Val