Canonical Allele Identifier: CA2579585170
Gene: TSPAN7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675693C>A , CM000685.2:g.38675693C>A GRCh38
NC_000023.10:g.38534947C>A , CM000685.1:g.38534947C>A GRCh37
NC_000023.9:g.38419891C>A NCBI36
NG_009160.1:g.119217C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378482.7:c.442-12C>A MANE Select ENSP00000367743.2:n.442-12C>A
ENST00000286824.6:c.493-12C>A ENSP00000286824.6:n.493-12C>A
ENST00000378482.6:c.442-12C>A ENSP00000367743.2:n.442-12C>A
ENST00000419600.3:n.386-12C>A
ENST00000465127.1:c.532-12C>A ENSP00000417050.1:n.532-12C>A
ENST00000471410.5:c.*468-12C>A ENSP00000419290.1:n.*468-12C>A
ENST00000475216.5:c.*435-12C>A ENSP00000418586.1:n.*435-12C>A
ENST00000488893.5:n.625-12C>A
NM_004615.3:c.442-12C>A NP_004606.2:n.442-12C>A
NM_004615.4:c.442-12C>A MANE Select NP_004606.2:n.442-12C>A
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