Canonical Allele Identifier: CA2820495034

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675967_38675968del , CM000685.2:g.38675967_38675968del	GRCh38
NC_000023.10:g.38535221_38535222del , CM000685.1:g.38535221_38535222del	GRCh37
NC_000023.9:g.38420165_38420166del	NCBI36
NG_009160.1:g.119491_119492del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+107_597+108del MANE Select	ENSP00000367743.2:n.597+107_597+108del
ENST00000286824.6:c.648+107_648+108del	ENSP00000286824.6:n.648+107_648+108del
ENST00000378482.6:c.597+107_597+108del	ENSP00000367743.2:n.597+107_597+108del
ENST00000419600.3:n.541+107_541+108del
ENST00000465127.1:c.687+107_687+108del	ENSP00000417050.1:n.687+107_687+108del
ENST00000471410.5:c.*623+107_*623+108del	ENSP00000419290.1:n.*623+107_*623+108del
ENST00000475216.5:c.*590+107_*590+108del	ENSP00000418586.1:n.*590+107_*590+108del
NM_004615.3:c.597+107_597+108del	NP_004606.2:n.597+107_597+108del
NM_004615.4:c.597+107_597+108del MANE Select	NP_004606.2:n.597+107_597+108del