Canonical Allele Identifier: CA2424970100

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675938_38675942delinsCAAAT , CM000685.2:g.38675938_38675942delinsCAAAT	GRCh38
NC_000023.10:g.38535192_38535196delinsCAAAT , CM000685.1:g.38535192_38535196delinsCAAAT	GRCh37
NC_000023.9:g.38420136_38420140delinsCAAAT	NCBI36
NG_009160.1:g.119462_119466delinsCAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+78_597+82delinsCAAAT MANE Select	ENSP00000367743.2:n.597+78_597+82delinsCAAAT
ENST00000286824.6:c.648+78_648+82delinsCAAAT	ENSP00000286824.6:n.648+78_648+82delinsCAAAT
ENST00000378482.6:c.597+78_597+82delinsCAAAT	ENSP00000367743.2:n.597+78_597+82delinsCAAAT
ENST00000419600.3:n.541+78_541+82delinsCAAAT
ENST00000465127.1:c.687+78_687+82delinsCAAAT	ENSP00000417050.1:n.687+78_687+82delinsCAAAT
ENST00000471410.5:c.*623+78_*623+82delinsCAAAT	ENSP00000419290.1:n.*623+78_*623+82delinsCAAAT
ENST00000475216.5:c.*590+78_*590+82delinsCAAAT	ENSP00000418586.1:n.*590+78_*590+82delinsCAAAT
NM_004615.3:c.597+78_597+82delinsCAAAT	NP_004606.2:n.597+78_597+82delinsCAAAT
NM_004615.4:c.597+78_597+82delinsCAAAT MANE Select	NP_004606.2:n.597+78_597+82delinsCAAAT