Canonical Allele Identifier: CA412982331
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675829T>G , CM000685.2:g.38675829T>G GRCh38
NC_000023.10:g.38535083T>G , CM000685.1:g.38535083T>G GRCh37
NC_000023.9:g.38420027T>G NCBI36
NG_009160.1:g.119353T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.566T>G MANE Select ENSP00000367743.2:p.Leu189Arg
ENST00000286824.6:c.617T>G ENSP00000286824.6:p.Leu206Arg
ENST00000378482.6:c.566T>G ENSP00000367743.2:p.Leu189Arg
ENST00000419600.3:n.510T>G
ENST00000465127.1:c.656T>G ENSP00000417050.1:p.Leu219Arg
ENST00000471410.5:c.*592T>G ENSP00000419290.1:n.*592T>G
ENST00000475216.5:c.*559T>G ENSP00000418586.1:n.*559T>G
NM_004615.3:c.566T>G NP_004606.2:p.Leu189Arg
NM_004615.4:c.566T>G MANE Select NP_004606.2:p.Leu189Arg