Canonical Allele Identifier: CA2424970082

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675896_38675897delinsGT , CM000685.2:g.38675896_38675897delinsGT	GRCh38
NC_000023.10:g.38535150_38535151delinsGT , CM000685.1:g.38535150_38535151delinsGT	GRCh37
NC_000023.9:g.38420094_38420095delinsGT	NCBI36
NG_009160.1:g.119420_119421delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+36_597+37delinsGT MANE Select	ENSP00000367743.2:n.597+36_597+37delinsGT
ENST00000286824.6:c.648+36_648+37delinsGT	ENSP00000286824.6:n.648+36_648+37delinsGT
ENST00000378482.6:c.597+36_597+37delinsGT	ENSP00000367743.2:n.597+36_597+37delinsGT
ENST00000419600.3:n.541+36_541+37delinsGT
ENST00000465127.1:c.687+36_687+37delinsGT	ENSP00000417050.1:n.687+36_687+37delinsGT
ENST00000471410.5:c.*623+36_*623+37delinsGT	ENSP00000419290.1:n.*623+36_*623+37delinsGT
ENST00000475216.5:c.*590+36_*590+37delinsGT	ENSP00000418586.1:n.*590+36_*590+37delinsGT
NM_004615.3:c.597+36_597+37delinsGT	NP_004606.2:n.597+36_597+37delinsGT
NM_004615.4:c.597+36_597+37delinsGT MANE Select	NP_004606.2:n.597+36_597+37delinsGT