Canonical Allele Identifier: CA2693446520

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675668-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675668T>G , CM000685.2:g.38675668T>G	GRCh38
NC_000023.10:g.38534922T>G , CM000685.1:g.38534922T>G	GRCh37
NC_000023.9:g.38419866T>G	NCBI36
NG_009160.1:g.119192T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-37T>G MANE Select	ENSP00000367743.2:n.442-37T>G
ENST00000286824.6:c.493-37T>G	ENSP00000286824.6:n.493-37T>G
ENST00000378482.6:c.442-37T>G	ENSP00000367743.2:n.442-37T>G
ENST00000419600.3:n.386-37T>G
ENST00000465127.1:c.532-37T>G	ENSP00000417050.1:n.532-37T>G
ENST00000471410.5:c.*468-37T>G	ENSP00000419290.1:n.*468-37T>G
ENST00000475216.5:c.*435-37T>G	ENSP00000418586.1:n.*435-37T>G
ENST00000488893.5:n.625-37T>G
NM_004615.3:c.442-37T>G	NP_004606.2:n.442-37T>G
NM_004615.4:c.442-37T>G MANE Select	NP_004606.2:n.442-37T>G