Canonical Allele Identifier: CA2424970032

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675709G= , CM000685.2:g.38675709G=	GRCh38
NC_000023.10:g.38534963G= , CM000685.1:g.38534963G=	GRCh37
NC_000023.9:g.38419907G=	NCBI36
NG_009160.1:g.119233G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378482.7:c.446G= MANE Select	ENSP00000367743.2:p.Ser149=
ENST00000286824.6:c.497G=	ENSP00000286824.6:p.Ser166=
ENST00000378482.6:c.446G=	ENSP00000367743.2:p.Ser149=
ENST00000419600.3:n.390G=
ENST00000465127.1:c.536G=	ENSP00000417050.1:p.Ser179=
ENST00000471410.5:c.*472G=	ENSP00000419290.1:n.*472G=
ENST00000475216.5:c.*439G=	ENSP00000418586.1:n.*439G=
ENST00000488893.5:n.629G=
NM_004615.3:c.446G=	NP_004606.2:p.Ser149=
NM_004615.4:c.446G= MANE Select	NP_004606.2:p.Ser149=