Canonical Allele Identifier: CA412982285

Gene: TSPAN7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.545A>C MANE Select	ENSP00000367743.2:p.Asn182Thr
ENST00000286824.6:c.596A>C	ENSP00000286824.6:p.Asn199Thr
ENST00000378482.6:c.545A>C	ENSP00000367743.2:p.Asn182Thr
ENST00000419600.3:n.489A>C
ENST00000465127.1:c.635A>C	ENSP00000417050.1:p.Asn212Thr
ENST00000471410.5:c.*571A>C	ENSP00000419290.1:n.*571A>C
ENST00000475216.5:c.*538A>C	ENSP00000418586.1:n.*538A>C
ENST00000488893.5:n.728A>C
NM_004615.3:c.545A>C	NP_004606.2:p.Asn182Thr
NM_004615.4:c.545A>C MANE Select	NP_004606.2:p.Asn182Thr