Canonical Allele Identifier: CA2579585164
Gene: TSPAN7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675632G>A , CM000685.2:g.38675632G>A GRCh38
NC_000023.10:g.38534886G>A , CM000685.1:g.38534886G>A GRCh37
NC_000023.9:g.38419830G>A NCBI36
NG_009160.1:g.119156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.442-73G>A MANE Select ENSP00000367743.2:n.442-73G>A
ENST00000286824.6:c.493-73G>A ENSP00000286824.6:n.493-73G>A
ENST00000378482.6:c.442-73G>A ENSP00000367743.2:n.442-73G>A
ENST00000419600.3:n.386-73G>A
ENST00000465127.1:c.532-73G>A ENSP00000417050.1:n.532-73G>A
ENST00000471410.5:c.*468-73G>A ENSP00000419290.1:n.*468-73G>A
ENST00000475216.5:c.*435-73G>A ENSP00000418586.1:n.*435-73G>A
ENST00000488893.5:n.625-73G>A
NM_004615.3:c.442-73G>A NP_004606.2:n.442-73G>A
NM_004615.4:c.442-73G>A MANE Select NP_004606.2:n.442-73G>A