Canonical Allele Identifier: CA412982311
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675820T>C , CM000685.2:g.38675820T>C GRCh38
NC_000023.10:g.38535074T>C , CM000685.1:g.38535074T>C GRCh37
NC_000023.9:g.38420018T>C NCBI36
NG_009160.1:g.119344T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.557T>C MANE Select ENSP00000367743.2:p.Leu186Pro
ENST00000286824.6:c.608T>C ENSP00000286824.6:p.Leu203Pro
ENST00000378482.6:c.557T>C ENSP00000367743.2:p.Leu186Pro
ENST00000419600.3:n.501T>C
ENST00000465127.1:c.647T>C ENSP00000417050.1:p.Leu216Pro
ENST00000471410.5:c.*583T>C ENSP00000419290.1:n.*583T>C
ENST00000475216.5:c.*550T>C ENSP00000418586.1:n.*550T>C
NM_004615.3:c.557T>C NP_004606.2:p.Leu186Pro
NM_004615.4:c.557T>C MANE Select NP_004606.2:p.Leu186Pro