Canonical Allele Identifier: CA2579585163
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675631del , CM000685.2:g.38675631del GRCh38
NC_000023.10:g.38534885del , CM000685.1:g.38534885del GRCh37
NC_000023.9:g.38419829del NCBI36
NG_009160.1:g.119155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-74del MANE Select ENSP00000367743.2:n.442-74del
ENST00000286824.6:c.493-74del ENSP00000286824.6:n.493-74del
ENST00000378482.6:c.442-74del ENSP00000367743.2:n.442-74del
ENST00000419600.3:n.386-74del
ENST00000465127.1:c.532-74del ENSP00000417050.1:n.532-74del
ENST00000471410.5:c.*468-74del ENSP00000419290.1:n.*468-74del
ENST00000475216.5:c.*435-74del ENSP00000418586.1:n.*435-74del
ENST00000488893.5:n.625-74del
NM_004615.3:c.442-74del NP_004606.2:n.442-74del
NM_004615.4:c.442-74del MANE Select NP_004606.2:n.442-74del