Canonical Allele Identifier: CA412982347

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675838-C-A
• MyVariant Identifiers: chrX:g.38535092C>A (hg19) ; chrX:g.38675838C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675838C>A , CM000685.2:g.38675838C>A	GRCh38
NC_000023.10:g.38535092C>A , CM000685.1:g.38535092C>A	GRCh37
NC_000023.9:g.38420036C>A	NCBI36
NG_009160.1:g.119362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.575C>A MANE Select	ENSP00000367743.2:p.Ala192Asp
ENST00000286824.6:c.626C>A	ENSP00000286824.6:p.Ala209Asp
ENST00000378482.6:c.575C>A	ENSP00000367743.2:p.Ala192Asp
ENST00000419600.3:n.519C>A
ENST00000465127.1:c.665C>A	ENSP00000417050.1:p.Ala222Asp
ENST00000471410.5:c.*601C>A	ENSP00000419290.1:n.*601C>A
ENST00000475216.5:c.*568C>A	ENSP00000418586.1:n.*568C>A
NM_004615.3:c.575C>A	NP_004606.2:p.Ala192Asp
NM_004615.4:c.575C>A MANE Select	NP_004606.2:p.Ala192Asp