Canonical Allele Identifier: CA412982304
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675817A>G , CM000685.2:g.38675817A>G GRCh38
NC_000023.10:g.38535071A>G , CM000685.1:g.38535071A>G GRCh37
NC_000023.9:g.38420015A>G NCBI36
NG_009160.1:g.119341A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.554A>G MANE Select ENSP00000367743.2:p.Asp185Gly
ENST00000286824.6:c.605A>G ENSP00000286824.6:p.Asp202Gly
ENST00000378482.6:c.554A>G ENSP00000367743.2:p.Asp185Gly
ENST00000419600.3:n.498A>G
ENST00000465127.1:c.644A>G ENSP00000417050.1:p.Asp215Gly
ENST00000471410.5:c.*580A>G ENSP00000419290.1:n.*580A>G
ENST00000475216.5:c.*547A>G ENSP00000418586.1:n.*547A>G
NM_004615.3:c.554A>G NP_004606.2:p.Asp185Gly
NM_004615.4:c.554A>G MANE Select NP_004606.2:p.Asp185Gly