Canonical Allele Identifier: CA2693446590
Gene: TSPAN7 HGNC NCBI

Linked Data

gnomAD v4: X-38676011-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38676011C>A , CM000685.2:g.38676011C>A GRCh38
NC_000023.10:g.38535265C>A , CM000685.1:g.38535265C>A GRCh37
NC_000023.9:g.38420209C>A NCBI36
NG_009160.1:g.119535C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+151C>A MANE Select ENSP00000367743.2:n.597+151C>A
ENST00000286824.6:c.648+151C>A ENSP00000286824.6:n.648+151C>A
ENST00000378482.6:c.597+151C>A ENSP00000367743.2:n.597+151C>A
ENST00000419600.3:n.541+151C>A
ENST00000465127.1:c.687+151C>A ENSP00000417050.1:n.687+151C>A
ENST00000471410.5:c.*623+151C>A ENSP00000419290.1:n.*623+151C>A
ENST00000475216.5:c.*590+151C>A ENSP00000418586.1:n.*590+151C>A
NM_004615.3:c.597+151C>A NP_004606.2:n.597+151C>A
NM_004615.4:c.597+151C>A MANE Select NP_004606.2:n.597+151C>A
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