Canonical Allele Identifier: CA2424970094
Gene: TSPAN7 HGNC NCBI

Linked Data

dbSNP Id: rs4826996
gnomAD v4: X-38675920-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675920A>T , CM000685.2:g.38675920A>T GRCh38
NC_000023.10:g.38535174A>T , CM000685.1:g.38535174A>T GRCh37
NC_000023.9:g.38420118A>T NCBI36
NG_009160.1:g.119444A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+60A>T MANE Select ENSP00000367743.2:n.597+60A>T
ENST00000286824.6:c.648+60A>T ENSP00000286824.6:n.648+60A>T
ENST00000378482.6:c.597+60A>T ENSP00000367743.2:n.597+60A>T
ENST00000419600.3:n.541+60A>T
ENST00000465127.1:c.687+60A>T ENSP00000417050.1:n.687+60A>T
ENST00000471410.5:c.*623+60A>T ENSP00000419290.1:n.*623+60A>T
ENST00000475216.5:c.*590+60A>T ENSP00000418586.1:n.*590+60A>T
NM_004615.3:c.597+60A>T NP_004606.2:n.597+60A>T
NM_004615.4:c.597+60A>T MANE Select NP_004606.2:n.597+60A>T
Search 100 bp 5'
Search 100 bp 3'