Canonical Allele Identifier: CA2424970065
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675819C= , CM000685.2:g.38675819C= GRCh38
NC_000023.10:g.38535073C= , CM000685.1:g.38535073C= GRCh37
NC_000023.9:g.38420017C= NCBI36
NG_009160.1:g.119343C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.556C= MANE Select ENSP00000367743.2:p.Leu186=
ENST00000286824.6:c.607C= ENSP00000286824.6:p.Leu203=
ENST00000378482.6:c.556C= ENSP00000367743.2:p.Leu186=
ENST00000419600.3:n.500C=
ENST00000465127.1:c.646C= ENSP00000417050.1:p.Leu216=
ENST00000471410.5:c.*582C= ENSP00000419290.1:n.*582C=
ENST00000475216.5:c.*549C= ENSP00000418586.1:n.*549C=
NM_004615.3:c.556C= NP_004606.2:p.Leu186=
NM_004615.4:c.556C= MANE Select NP_004606.2:p.Leu186=