Canonical Allele Identifier: CA1917819226

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1841842996

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485902_69485906del , CM000672.2:g.69485902_69485906del	GRCh38
NC_000010.10:g.71245658_71245662del , CM000672.1:g.71245658_71245662del	GRCh37
NC_000010.9:g.70915664_70915668del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+687_357+691del MANE Select	ENSP00000362387.2:n.357+687_357+691del
ENST00000373290.6:c.357+687_357+691del	ENSP00000362387.2:n.357+687_357+691del
ENST00000452130.1:c.84+687_84+691del	ENSP00000404528.1:n.84+687_84+691del
ENST00000475069.5:n.127+687_127+691del
NM_012339.3:c.357+687_357+691del	NP_036471.1:n.357+687_357+691del
XM_005269667.3:c.97-9692_97-9688del	XP_005269724.1:n.97-9692_97-9688del
XM_006717738.2:c.285+687_285+691del	XP_006717801.1:n.285+687_285+691del
XR_945642.1:n.487+687_487+691del
NM_001351263.1:c.97-9692_97-9688del	NP_001338192.1:n.97-9692_97-9688del
NM_012339.4:c.357+687_357+691del	NP_036471.1:n.357+687_357+691del
NR_147091.1:n.485+687_485+691del
XM_017016010.1:c.357+687_357+691del	XP_016871499.1:n.357+687_357+691del
XR_001747072.1:n.488+687_488+691del
XR_001747073.1:n.488+687_488+691del
XR_001747074.1:n.485+687_485+691del
NM_012339.5:c.357+687_357+691del MANE Select	NP_036471.1:n.357+687_357+691del
NM_001351263.2:c.97-9692_97-9688del	NP_001338192.1:n.97-9692_97-9688del
NR_147091.2:n.487+687_487+691del