Canonical Allele Identifier: CA412982354
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675841C>T , CM000685.2:g.38675841C>T GRCh38
NC_000023.10:g.38535095C>T , CM000685.1:g.38535095C>T GRCh37
NC_000023.9:g.38420039C>T NCBI36
NG_009160.1:g.119365C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.578C>T MANE Select ENSP00000367743.2:p.Ala193Val
ENST00000286824.6:c.629C>T ENSP00000286824.6:p.Ala210Val
ENST00000378482.6:c.578C>T ENSP00000367743.2:p.Ala193Val
ENST00000419600.3:n.522C>T
ENST00000465127.1:c.668C>T ENSP00000417050.1:p.Ala223Val
ENST00000471410.5:c.*604C>T ENSP00000419290.1:n.*604C>T
ENST00000475216.5:c.*571C>T ENSP00000418586.1:n.*571C>T
NM_004615.3:c.578C>T NP_004606.2:p.Ala193Val
NM_004615.4:c.578C>T MANE Select NP_004606.2:p.Ala193Val