Canonical Allele Identifier: CA328161121
Gene: TSPAN7 HGNC NCBI

Linked Data

dbSNP Id: rs968461936
gnomAD v4: X-38676007-G-A
MyVariant Identifiers: chrX:g.38535261G>A (hg19) chrX:g.38676007G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38676007G>A , CM000685.2:g.38676007G>A GRCh38
NC_000023.10:g.38535261G>A , CM000685.1:g.38535261G>A GRCh37
NC_000023.9:g.38420205G>A NCBI36
NG_009160.1:g.119531G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+147G>A MANE Select ENSP00000367743.2:n.597+147G>A
ENST00000286824.6:c.648+147G>A ENSP00000286824.6:n.648+147G>A
ENST00000378482.6:c.597+147G>A ENSP00000367743.2:n.597+147G>A
ENST00000419600.3:n.541+147G>A
ENST00000465127.1:c.687+147G>A ENSP00000417050.1:n.687+147G>A
ENST00000471410.5:c.*623+147G>A ENSP00000419290.1:n.*623+147G>A
ENST00000475216.5:c.*590+147G>A ENSP00000418586.1:n.*590+147G>A
NM_004615.3:c.597+147G>A NP_004606.2:n.597+147G>A
NM_004615.4:c.597+147G>A MANE Select NP_004606.2:n.597+147G>A
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