Canonical Allele Identifier: CA412982349

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535092C>T (hg19) ; chrX:g.38675838C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.575C>T MANE Select	ENSP00000367743.2:p.Ala192Val
ENST00000286824.6:c.626C>T	ENSP00000286824.6:p.Ala209Val
ENST00000378482.6:c.575C>T	ENSP00000367743.2:p.Ala192Val
ENST00000419600.3:n.519C>T
ENST00000465127.1:c.665C>T	ENSP00000417050.1:p.Ala222Val
ENST00000471410.5:c.*601C>T	ENSP00000419290.1:n.*601C>T
ENST00000475216.5:c.*568C>T	ENSP00000418586.1:n.*568C>T
NM_004615.3:c.575C>T	NP_004606.2:p.Ala192Val
NM_004615.4:c.575C>T MANE Select	NP_004606.2:p.Ala192Val