Canonical Allele Identifier: CA1917807491

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1841158955

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69458261_69458262insGA , CM000672.2:g.69458261_69458262insGA	GRCh38
NC_000010.10:g.71218017_71218018insGA , CM000672.1:g.71218017_71218018insGA	GRCh37
NC_000010.9:g.70888023_70888024insGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.96+6571_96+6572insGA MANE Select	ENSP00000362387.2:n.96+6571_96+6572insGA
ENST00000373290.6:c.96+6571_96+6572insGA	ENSP00000362387.2:n.96+6571_96+6572insGA
ENST00000478112.1:n.214+6571_214+6572insGA
NM_012339.3:c.96+6571_96+6572insGA	NP_036471.1:n.96+6571_96+6572insGA
XM_005269667.3:c.96+6571_96+6572insGA	XP_005269724.1:n.96+6571_96+6572insGA
XM_006717738.2:c.25-25430_25-25429insGA	XP_006717801.1:n.25-25430_25-25429insGA
XR_945642.1:n.226+6571_226+6572insGA
NM_001351263.1:c.96+6571_96+6572insGA	NP_001338192.1:n.96+6571_96+6572insGA
NM_012339.4:c.96+6571_96+6572insGA	NP_036471.1:n.96+6571_96+6572insGA
NR_147091.1:n.224+6571_224+6572insGA
XM_017016010.1:c.96+6571_96+6572insGA	XP_016871499.1:n.96+6571_96+6572insGA
XR_001747072.1:n.227+6571_227+6572insGA
XR_001747073.1:n.227+6571_227+6572insGA
XR_001747074.1:n.224+6571_224+6572insGA
NM_012339.5:c.96+6571_96+6572insGA MANE Select	NP_036471.1:n.96+6571_96+6572insGA
NM_001351263.2:c.96+6571_96+6572insGA	NP_001338192.1:n.96+6571_96+6572insGA
NR_147091.2:n.226+6571_226+6572insGA