Canonical Allele Identifier: CA10386108

Gene: TSPAN7

Linked Data

• dbSNP Id: rs190004633
• ExAC: X:38534933 T / A
• gnomAD v2: X-38534933-T-A
• gnomAD v3: X-38675679-T-A
• gnomAD v4: X-38675679-T-A
• MyVariant Identifiers: chrX:g.38534933T>A (hg19) ; chrX:g.38675679T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675679T>A , CM000685.2:g.38675679T>A	GRCh38
NC_000023.10:g.38534933T>A , CM000685.1:g.38534933T>A	GRCh37
NC_000023.9:g.38419877T>A	NCBI36
NG_009160.1:g.119203T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-26T>A MANE Select	ENSP00000367743.2:n.442-26T>A
ENST00000286824.6:c.493-26T>A	ENSP00000286824.6:n.493-26T>A
ENST00000378482.6:c.442-26T>A	ENSP00000367743.2:n.442-26T>A
ENST00000419600.3:n.386-26T>A
ENST00000465127.1:c.532-26T>A	ENSP00000417050.1:n.532-26T>A
ENST00000471410.5:c.*468-26T>A	ENSP00000419290.1:n.*468-26T>A
ENST00000475216.5:c.*435-26T>A	ENSP00000418586.1:n.*435-26T>A
ENST00000488893.5:n.625-26T>A
NM_004615.3:c.442-26T>A	NP_004606.2:n.442-26T>A
NM_004615.4:c.442-26T>A MANE Select	NP_004606.2:n.442-26T>A