Canonical Allele Identifier: CA515685541
Gene: TSPAN7 HGNC NCBI

Linked Data

gnomAD v4: X-38675905-T-C
MyVariant Identifiers: chrX:g.38535159T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675905T>C , CM000685.2:g.38675905T>C GRCh38
NC_000023.10:g.38535159T>C , CM000685.1:g.38535159T>C GRCh37
NC_000023.9:g.38420103T>C NCBI36
NG_009160.1:g.119429T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+45T>C MANE Select ENSP00000367743.2:n.597+45T>C
ENST00000286824.6:c.648+45T>C ENSP00000286824.6:n.648+45T>C
ENST00000378482.6:c.597+45T>C ENSP00000367743.2:n.597+45T>C
ENST00000419600.3:n.541+45T>C
ENST00000465127.1:c.687+45T>C ENSP00000417050.1:n.687+45T>C
ENST00000471410.5:c.*623+45T>C ENSP00000419290.1:n.*623+45T>C
ENST00000475216.5:c.*590+45T>C ENSP00000418586.1:n.*590+45T>C
NM_004615.3:c.597+45T>C NP_004606.2:n.597+45T>C
NM_004615.4:c.597+45T>C MANE Select NP_004606.2:n.597+45T>C
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