Canonical Allele Identifier: CA875200438
Gene: TSPAN7 HGNC NCBI

Linked Data

dbSNP Id: rs1178857427
gnomAD v4: X-38676010-A-C
MyVariant Identifiers: chrX:g.38535264A>C (hg19) chrX:g.38676010A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38676010A>C , CM000685.2:g.38676010A>C GRCh38
NC_000023.10:g.38535264A>C , CM000685.1:g.38535264A>C GRCh37
NC_000023.9:g.38420208A>C NCBI36
NG_009160.1:g.119534A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.597+150A>C MANE Select ENSP00000367743.2:n.597+150A>C
ENST00000286824.6:c.648+150A>C ENSP00000286824.6:n.648+150A>C
ENST00000378482.6:c.597+150A>C ENSP00000367743.2:n.597+150A>C
ENST00000419600.3:n.541+150A>C
ENST00000465127.1:c.687+150A>C ENSP00000417050.1:n.687+150A>C
ENST00000471410.5:c.*623+150A>C ENSP00000419290.1:n.*623+150A>C
ENST00000475216.5:c.*590+150A>C ENSP00000418586.1:n.*590+150A>C
NM_004615.3:c.597+150A>C NP_004606.2:n.597+150A>C
NM_004615.4:c.597+150A>C MANE Select NP_004606.2:n.597+150A>C
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