Canonical Allele Identifier: CA2693446474
Gene: TSPAN7 HGNC NCBI

Linked Data

gnomAD v4: X-38675557-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675557G>A , CM000685.2:g.38675557G>A GRCh38
NC_000023.10:g.38534811G>A , CM000685.1:g.38534811G>A GRCh37
NC_000023.9:g.38419755G>A NCBI36
NG_009160.1:g.119081G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-148G>A MANE Select ENSP00000367743.2:n.442-148G>A
ENST00000286824.6:c.493-148G>A ENSP00000286824.6:n.493-148G>A
ENST00000378482.6:c.442-148G>A ENSP00000367743.2:n.442-148G>A
ENST00000419600.3:n.386-148G>A
ENST00000465127.1:c.532-148G>A ENSP00000417050.1:n.532-148G>A
ENST00000471410.5:c.*468-148G>A ENSP00000419290.1:n.*468-148G>A
ENST00000475216.5:c.*435-148G>A ENSP00000418586.1:n.*435-148G>A
ENST00000488893.5:n.625-148G>A
NM_004615.3:c.442-148G>A NP_004606.2:n.442-148G>A
NM_004615.4:c.442-148G>A MANE Select NP_004606.2:n.442-148G>A
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