Canonical Allele Identifier: CA209249434

Gene: TSPAN15

Linked Data

• dbSNP Id: rs867825760
• MyVariant Identifiers: chr10:g.71218018A>G (hg19) ; chr10:g.69458262A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69458262A>G , CM000672.2:g.69458262A>G	GRCh38
NC_000010.10:g.71218018A>G , CM000672.1:g.71218018A>G	GRCh37
NC_000010.9:g.70888024A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.96+6572A>G MANE Select	ENSP00000362387.2:n.96+6572A>G
ENST00000373290.6:c.96+6572A>G	ENSP00000362387.2:n.96+6572A>G
ENST00000478112.1:n.214+6572A>G
NM_012339.3:c.96+6572A>G	NP_036471.1:n.96+6572A>G
XM_005269667.3:c.96+6572A>G	XP_005269724.1:n.96+6572A>G
XM_006717738.2:c.25-25429A>G	XP_006717801.1:n.25-25429A>G
XR_945642.1:n.226+6572A>G
NM_001351263.1:c.96+6572A>G	NP_001338192.1:n.96+6572A>G
NM_012339.4:c.96+6572A>G	NP_036471.1:n.96+6572A>G
NR_147091.1:n.224+6572A>G
XM_017016010.1:c.96+6572A>G	XP_016871499.1:n.96+6572A>G
XR_001747072.1:n.227+6572A>G
XR_001747073.1:n.227+6572A>G
XR_001747074.1:n.224+6572A>G
NM_012339.5:c.96+6572A>G MANE Select	NP_036471.1:n.96+6572A>G
NM_001351263.2:c.96+6572A>G	NP_001338192.1:n.96+6572A>G
NR_147091.2:n.226+6572A>G