Canonical Allele Identifier: CA412982284

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535062A>T (hg19) ; chrX:g.38675808A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675808A>T , CM000685.2:g.38675808A>T	GRCh38
NC_000023.10:g.38535062A>T , CM000685.1:g.38535062A>T	GRCh37
NC_000023.9:g.38420006A>T	NCBI36
NG_009160.1:g.119332A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.545A>T MANE Select	ENSP00000367743.2:p.Asn182Ile
ENST00000286824.6:c.596A>T	ENSP00000286824.6:p.Asn199Ile
ENST00000378482.6:c.545A>T	ENSP00000367743.2:p.Asn182Ile
ENST00000419600.3:n.489A>T
ENST00000465127.1:c.635A>T	ENSP00000417050.1:p.Asn212Ile
ENST00000471410.5:c.*571A>T	ENSP00000419290.1:n.*571A>T
ENST00000475216.5:c.*538A>T	ENSP00000418586.1:n.*538A>T
ENST00000488893.5:n.728A>T
NM_004615.3:c.545A>T	NP_004606.2:p.Asn182Ile
NM_004615.4:c.545A>T MANE Select	NP_004606.2:p.Asn182Ile