Canonical Allele Identifier: CA412982334

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535085A>T (hg19) ; chrX:g.38675831A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675831A>T , CM000685.2:g.38675831A>T	GRCh38
NC_000023.10:g.38535085A>T , CM000685.1:g.38535085A>T	GRCh37
NC_000023.9:g.38420029A>T	NCBI36
NG_009160.1:g.119355A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.568A>T MANE Select	ENSP00000367743.2:p.Thr190Ser
ENST00000286824.6:c.619A>T	ENSP00000286824.6:p.Thr207Ser
ENST00000378482.6:c.568A>T	ENSP00000367743.2:p.Thr190Ser
ENST00000419600.3:n.512A>T
ENST00000465127.1:c.658A>T	ENSP00000417050.1:p.Thr220Ser
ENST00000471410.5:c.*594A>T	ENSP00000419290.1:n.*594A>T
ENST00000475216.5:c.*561A>T	ENSP00000418586.1:n.*561A>T
NM_004615.3:c.568A>T	NP_004606.2:p.Thr190Ser
NM_004615.4:c.568A>T MANE Select	NP_004606.2:p.Thr190Ser