Canonical Allele Identifier: CA2693446530
Gene: TSPAN7 HGNC NCBI

Linked Data

gnomAD v4: X-38675898-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675898G>A , CM000685.2:g.38675898G>A GRCh38
NC_000023.10:g.38535152G>A , CM000685.1:g.38535152G>A GRCh37
NC_000023.9:g.38420096G>A NCBI36
NG_009160.1:g.119422G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+38G>A MANE Select ENSP00000367743.2:n.597+38G>A
ENST00000286824.6:c.648+38G>A ENSP00000286824.6:n.648+38G>A
ENST00000378482.6:c.597+38G>A ENSP00000367743.2:n.597+38G>A
ENST00000419600.3:n.541+38G>A
ENST00000465127.1:c.687+38G>A ENSP00000417050.1:n.687+38G>A
ENST00000471410.5:c.*623+38G>A ENSP00000419290.1:n.*623+38G>A
ENST00000475216.5:c.*590+38G>A ENSP00000418586.1:n.*590+38G>A
NM_004615.3:c.597+38G>A NP_004606.2:n.597+38G>A
NM_004615.4:c.597+38G>A MANE Select NP_004606.2:n.597+38G>A
Search 100 bp 5'
Search 100 bp 3'