Canonical Allele Identifier: CA2693446557

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675938-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675940_38675941del , CM000685.2:g.38675940_38675941del	GRCh38
NC_000023.10:g.38535194_38535195del , CM000685.1:g.38535194_38535195del	GRCh37
NC_000023.9:g.38420138_38420139del	NCBI36
NG_009160.1:g.119464_119465del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+80_597+81del MANE Select	ENSP00000367743.2:n.597+80_597+81del
ENST00000286824.6:c.648+80_648+81del	ENSP00000286824.6:n.648+80_648+81del
ENST00000378482.6:c.597+80_597+81del	ENSP00000367743.2:n.597+80_597+81del
ENST00000419600.3:n.541+80_541+81del
ENST00000465127.1:c.687+80_687+81del	ENSP00000417050.1:n.687+80_687+81del
ENST00000471410.5:c.*623+80_*623+81del	ENSP00000419290.1:n.*623+80_*623+81del
ENST00000475216.5:c.*590+80_*590+81del	ENSP00000418586.1:n.*590+80_*590+81del
NM_004615.3:c.597+80_597+81del	NP_004606.2:n.597+80_597+81del
NM_004615.4:c.597+80_597+81del MANE Select	NP_004606.2:n.597+80_597+81del