Canonical Allele Identifier: CA2424969999
Gene: TSPAN7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675575A= , CM000685.2:g.38675575A= GRCh38
NC_000023.10:g.38534829A= , CM000685.1:g.38534829A= GRCh37
NC_000023.9:g.38419773A= NCBI36
NG_009160.1:g.119099A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-130A= MANE Select ENSP00000367743.2:n.442-130A=
ENST00000286824.6:c.493-130A= ENSP00000286824.6:n.493-130A=
ENST00000378482.6:c.442-130A= ENSP00000367743.2:n.442-130A=
ENST00000419600.3:n.386-130A=
ENST00000465127.1:c.532-130A= ENSP00000417050.1:n.532-130A=
ENST00000471410.5:c.*468-130A= ENSP00000419290.1:n.*468-130A=
ENST00000475216.5:c.*435-130A= ENSP00000418586.1:n.*435-130A=
ENST00000488893.5:n.625-130A=
NM_004615.3:c.442-130A= NP_004606.2:n.442-130A=
NM_004615.4:c.442-130A= MANE Select NP_004606.2:n.442-130A=
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