Canonical Allele Identifier: CA412982035
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38534957A>G (hg19) chrX:g.38675703A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675703A>G , CM000685.2:g.38675703A>G GRCh38
NC_000023.10:g.38534957A>G , CM000685.1:g.38534957A>G GRCh37
NC_000023.9:g.38419901A>G NCBI36
NG_009160.1:g.119227A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378482.7:c.442-2A>G MANE Select ENSP00000367743.2:n.442-2A>G
ENST00000286824.6:c.493-2A>G ENSP00000286824.6:n.493-2A>G
ENST00000378482.6:c.442-2A>G ENSP00000367743.2:n.442-2A>G
ENST00000419600.3:n.386-2A>G
ENST00000465127.1:c.532-2A>G ENSP00000417050.1:n.532-2A>G
ENST00000471410.5:c.*468-2A>G ENSP00000419290.1:n.*468-2A>G
ENST00000475216.5:c.*435-2A>G ENSP00000418586.1:n.*435-2A>G
ENST00000488893.5:n.625-2A>G
NM_004615.3:c.442-2A>G NP_004606.2:n.442-2A>G
NM_004615.4:c.442-2A>G MANE Select NP_004606.2:n.442-2A>G
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Search 100 bp 3'