Canonical Allele Identifier: CA2424970110

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675974_38675978delinsTCTTA , CM000685.2:g.38675974_38675978delinsTCTTA	GRCh38
NC_000023.10:g.38535228_38535232delinsTCTTA , CM000685.1:g.38535228_38535232delinsTCTTA	GRCh37
NC_000023.9:g.38420172_38420176delinsTCTTA	NCBI36
NG_009160.1:g.119498_119502delinsTCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+114_597+118delinsTCTTA MANE Select	ENSP00000367743.2:n.597+114_597+118delinsTCTTA
ENST00000286824.6:c.648+114_648+118delinsTCTTA	ENSP00000286824.6:n.648+114_648+118delinsTCTTA
ENST00000378482.6:c.597+114_597+118delinsTCTTA	ENSP00000367743.2:n.597+114_597+118delinsTCTTA
ENST00000419600.3:n.541+114_541+118delinsTCTTA
ENST00000465127.1:c.687+114_687+118delinsTCTTA	ENSP00000417050.1:n.687+114_687+118delinsTCTTA
ENST00000471410.5:c.*623+114_*623+118delinsTCTTA	ENSP00000419290.1:n.*623+114_*623+118delinsTCTTA
ENST00000475216.5:c.*590+114_*590+118delinsTCTTA	ENSP00000418586.1:n.*590+114_*590+118delinsTCTTA
NM_004615.3:c.597+114_597+118delinsTCTTA	NP_004606.2:n.597+114_597+118delinsTCTTA
NM_004615.4:c.597+114_597+118delinsTCTTA MANE Select	NP_004606.2:n.597+114_597+118delinsTCTTA