Canonical Allele Identifier: CA2424970072

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675854C= , CM000685.2:g.38675854C=	GRCh38
NC_000023.10:g.38535108C= , CM000685.1:g.38535108C=	GRCh37
NC_000023.9:g.38420052C=	NCBI36
NG_009160.1:g.119378C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.591C= MANE Select	ENSP00000367743.2:p.Asn197=
ENST00000286824.6:c.642C=	ENSP00000286824.6:p.Asn214=
ENST00000378482.6:c.591C=	ENSP00000367743.2:p.Asn197=
ENST00000419600.3:n.535C=
ENST00000465127.1:c.681C=	ENSP00000417050.1:p.Asn227=
ENST00000471410.5:c.*617C=	ENSP00000419290.1:n.*617C=
ENST00000475216.5:c.*584C=	ENSP00000418586.1:n.*584C=
NM_004615.3:c.591C=	NP_004606.2:p.Asn197=
NM_004615.4:c.591C= MANE Select	NP_004606.2:p.Asn197=