Canonical Allele Identifier: CA918700620

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1554833546

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485779_69485780delinsA , CM000672.2:g.69485779_69485780delinsA	GRCh38
NC_000010.10:g.71245535_71245536delinsA , CM000672.1:g.71245535_71245536delinsA	GRCh37
NC_000010.9:g.70915541_70915542delinsA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+564_357+565delinsA MANE Select	ENSP00000362387.2:n.357+564_357+565delinsA
ENST00000373290.6:c.357+564_357+565delinsA	ENSP00000362387.2:n.357+564_357+565delinsA
ENST00000452130.1:c.84+564_84+565delinsA	ENSP00000404528.1:n.84+564_84+565delinsA
ENST00000475069.5:n.127+564_127+565delinsA
NM_012339.3:c.357+564_357+565delinsA	NP_036471.1:n.357+564_357+565delinsA
XM_005269667.3:c.97-9815_97-9814delinsA	XP_005269724.1:n.97-9815_97-9814delinsA
XM_006717738.2:c.285+564_285+565delinsA	XP_006717801.1:n.285+564_285+565delinsA
XR_945642.1:n.487+564_487+565delinsA
NM_001351263.1:c.97-9815_97-9814delinsA	NP_001338192.1:n.97-9815_97-9814delinsA
NM_012339.4:c.357+564_357+565delinsA	NP_036471.1:n.357+564_357+565delinsA
NR_147091.1:n.485+564_485+565delinsA
XM_017016010.1:c.357+564_357+565delinsA	XP_016871499.1:n.357+564_357+565delinsA
XR_001747072.1:n.488+564_488+565delinsA
XR_001747073.1:n.488+564_488+565delinsA
XR_001747074.1:n.485+564_485+565delinsA
NM_012339.5:c.357+564_357+565delinsA MANE Select	NP_036471.1:n.357+564_357+565delinsA
NM_001351263.2:c.97-9815_97-9814delinsA	NP_001338192.1:n.97-9815_97-9814delinsA
NR_147091.2:n.487+564_487+565delinsA