Canonical Allele Identifier: CA2424970063

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675815G= , CM000685.2:g.38675815G=	GRCh38
NC_000023.10:g.38535069G= , CM000685.1:g.38535069G=	GRCh37
NC_000023.9:g.38420013G=	NCBI36
NG_009160.1:g.119339G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.552G= MANE Select	ENSP00000367743.2:p.Gln184=
ENST00000286824.6:c.603G=	ENSP00000286824.6:p.Gln201=
ENST00000378482.6:c.552G=	ENSP00000367743.2:p.Gln184=
ENST00000419600.3:n.496G=
ENST00000465127.1:c.642G=	ENSP00000417050.1:p.Gln214=
ENST00000471410.5:c.*578G=	ENSP00000419290.1:n.*578G=
ENST00000475216.5:c.*545G=	ENSP00000418586.1:n.*545G=
ENST00000488893.5:n.735G=
NM_004615.3:c.552G=	NP_004606.2:p.Gln184=
NM_004615.4:c.552G= MANE Select	NP_004606.2:p.Gln184=