Canonical Allele Identifier: CA2424969996
Gene: TSPAN7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675558A= , CM000685.2:g.38675558A= GRCh38
NC_000023.10:g.38534812A= , CM000685.1:g.38534812A= GRCh37
NC_000023.9:g.38419756A= NCBI36
NG_009160.1:g.119082A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-147A= MANE Select ENSP00000367743.2:n.442-147A=
ENST00000286824.6:c.493-147A= ENSP00000286824.6:n.493-147A=
ENST00000378482.6:c.442-147A= ENSP00000367743.2:n.442-147A=
ENST00000419600.3:n.386-147A=
ENST00000465127.1:c.532-147A= ENSP00000417050.1:n.532-147A=
ENST00000471410.5:c.*468-147A= ENSP00000419290.1:n.*468-147A=
ENST00000475216.5:c.*435-147A= ENSP00000418586.1:n.*435-147A=
ENST00000488893.5:n.625-147A=
NM_004615.3:c.442-147A= NP_004606.2:n.442-147A=
NM_004615.4:c.442-147A= MANE Select NP_004606.2:n.442-147A=
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