Canonical Allele Identifier: CA2788415996

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69458201T>A , CM000672.2:g.69458201T>A	GRCh38
NC_000010.10:g.71217957T>A , CM000672.1:g.71217957T>A	GRCh37
NC_000010.9:g.70887963T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.96+6511T>A MANE Select	ENSP00000362387.2:n.96+6511T>A
ENST00000373290.6:c.96+6511T>A	ENSP00000362387.2:n.96+6511T>A
ENST00000478112.1:n.214+6511T>A
NM_012339.3:c.96+6511T>A	NP_036471.1:n.96+6511T>A
XM_005269667.3:c.96+6511T>A	XP_005269724.1:n.96+6511T>A
XM_006717738.2:c.25-25490T>A	XP_006717801.1:n.25-25490T>A
XR_945642.1:n.226+6511T>A
NM_001351263.1:c.96+6511T>A	NP_001338192.1:n.96+6511T>A
NM_012339.4:c.96+6511T>A	NP_036471.1:n.96+6511T>A
NR_147091.1:n.224+6511T>A
XM_017016010.1:c.96+6511T>A	XP_016871499.1:n.96+6511T>A
XR_001747072.1:n.227+6511T>A
XR_001747073.1:n.227+6511T>A
XR_001747074.1:n.224+6511T>A
NM_012339.5:c.96+6511T>A MANE Select	NP_036471.1:n.96+6511T>A
NM_001351263.2:c.96+6511T>A	NP_001338192.1:n.96+6511T>A
NR_147091.2:n.226+6511T>A