Canonical Allele Identifier: CA412982187

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535020A>C (hg19) ; chrX:g.38675766A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675766A>C , CM000685.2:g.38675766A>C	GRCh38
NC_000023.10:g.38535020A>C , CM000685.1:g.38535020A>C	GRCh37
NC_000023.9:g.38419964A>C	NCBI36
NG_009160.1:g.119290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.503A>C MANE Select	ENSP00000367743.2:p.His168Pro
ENST00000286824.6:c.554A>C	ENSP00000286824.6:p.His185Pro
ENST00000378482.6:c.503A>C	ENSP00000367743.2:p.His168Pro
ENST00000419600.3:n.447A>C
ENST00000465127.1:c.593A>C	ENSP00000417050.1:p.His198Pro
ENST00000471410.5:c.*529A>C	ENSP00000419290.1:n.*529A>C
ENST00000475216.5:c.*496A>C	ENSP00000418586.1:n.*496A>C
ENST00000488893.5:n.686A>C
NM_004615.3:c.503A>C	NP_004606.2:p.His168Pro
NM_004615.4:c.503A>C MANE Select	NP_004606.2:p.His168Pro