Canonical Allele Identifier: CA2424970068

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675839C= , CM000685.2:g.38675839C=	GRCh38
NC_000023.10:g.38535093C= , CM000685.1:g.38535093C=	GRCh37
NC_000023.9:g.38420037C=	NCBI36
NG_009160.1:g.119363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.576C= MANE Select	ENSP00000367743.2:p.Ala192=
ENST00000286824.6:c.627C=	ENSP00000286824.6:p.Ala209=
ENST00000378482.6:c.576C=	ENSP00000367743.2:p.Ala192=
ENST00000419600.3:n.520C=
ENST00000465127.1:c.666C=	ENSP00000417050.1:p.Ala222=
ENST00000471410.5:c.*602C=	ENSP00000419290.1:n.*602C=
ENST00000475216.5:c.*569C=	ENSP00000418586.1:n.*569C=
NM_004615.3:c.576C=	NP_004606.2:p.Ala192=
NM_004615.4:c.576C= MANE Select	NP_004606.2:p.Ala192=