Canonical Allele Identifier: CA2499854803
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675679del , CM000685.2:g.38675679del GRCh38
NC_000023.10:g.38534933del , CM000685.1:g.38534933del GRCh37
NC_000023.9:g.38419877del NCBI36
NG_009160.1:g.119203del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-26del MANE Select ENSP00000367743.2:n.442-26del
ENST00000286824.6:c.493-26del ENSP00000286824.6:n.493-26del
ENST00000378482.6:c.442-26del ENSP00000367743.2:n.442-26del
ENST00000419600.3:n.386-26del
ENST00000465127.1:c.532-26del ENSP00000417050.1:n.532-26del
ENST00000471410.5:c.*468-26del ENSP00000419290.1:n.*468-26del
ENST00000475216.5:c.*435-26del ENSP00000418586.1:n.*435-26del
ENST00000488893.5:n.625-26del
NM_004615.3:c.442-26del NP_004606.2:n.442-26del
NM_004615.4:c.442-26del MANE Select NP_004606.2:n.442-26del