Canonical Allele Identifier: CA2693446499

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675613-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675617_38675618del , CM000685.2:g.38675617_38675618del	GRCh38
NC_000023.10:g.38534871_38534872del , CM000685.1:g.38534871_38534872del	GRCh37
NC_000023.9:g.38419815_38419816del	NCBI36
NG_009160.1:g.119141_119142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-88_442-87del MANE Select	ENSP00000367743.2:n.442-88_442-87del
ENST00000286824.6:c.493-88_493-87del	ENSP00000286824.6:n.493-88_493-87del
ENST00000378482.6:c.442-88_442-87del	ENSP00000367743.2:n.442-88_442-87del
ENST00000419600.3:n.386-88_386-87del
ENST00000465127.1:c.532-88_532-87del	ENSP00000417050.1:n.532-88_532-87del
ENST00000471410.5:c.*468-88_*468-87del	ENSP00000419290.1:n.*468-88_*468-87del
ENST00000475216.5:c.*435-88_*435-87del	ENSP00000418586.1:n.*435-88_*435-87del
ENST00000488893.5:n.625-88_625-87del
NM_004615.3:c.442-88_442-87del	NP_004606.2:n.442-88_442-87del
NM_004615.4:c.442-88_442-87del MANE Select	NP_004606.2:n.442-88_442-87del