Canonical Allele Identifier: CA2424970024
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675689C= , CM000685.2:g.38675689C= GRCh38
NC_000023.10:g.38534943C= , CM000685.1:g.38534943C= GRCh37
NC_000023.9:g.38419887C= NCBI36
NG_009160.1:g.119213C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-16C= MANE Select ENSP00000367743.2:n.442-16C=
ENST00000286824.6:c.493-16C= ENSP00000286824.6:n.493-16C=
ENST00000378482.6:c.442-16C= ENSP00000367743.2:n.442-16C=
ENST00000419600.3:n.386-16C=
ENST00000465127.1:c.532-16C= ENSP00000417050.1:n.532-16C=
ENST00000471410.5:c.*468-16C= ENSP00000419290.1:n.*468-16C=
ENST00000475216.5:c.*435-16C= ENSP00000418586.1:n.*435-16C=
ENST00000488893.5:n.625-16C=
NM_004615.3:c.442-16C= NP_004606.2:n.442-16C=
NM_004615.4:c.442-16C= MANE Select NP_004606.2:n.442-16C=