Canonical Allele Identifier: CA412982341
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675835T>C , CM000685.2:g.38675835T>C GRCh38
NC_000023.10:g.38535089T>C , CM000685.1:g.38535089T>C GRCh37
NC_000023.9:g.38420033T>C NCBI36
NG_009160.1:g.119359T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.572T>C MANE Select ENSP00000367743.2:p.Val191Ala
ENST00000286824.6:c.623T>C ENSP00000286824.6:p.Val208Ala
ENST00000378482.6:c.572T>C ENSP00000367743.2:p.Val191Ala
ENST00000419600.3:n.516T>C
ENST00000465127.1:c.662T>C ENSP00000417050.1:p.Val221Ala
ENST00000471410.5:c.*598T>C ENSP00000419290.1:n.*598T>C
ENST00000475216.5:c.*565T>C ENSP00000418586.1:n.*565T>C
NM_004615.3:c.572T>C NP_004606.2:p.Val191Ala
NM_004615.4:c.572T>C MANE Select NP_004606.2:p.Val191Ala