Canonical Allele Identifier: CA929627143

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1841840525
• gnomAD v3: 10-69485795-TGG-T
• gnomAD v4: 10-69485795-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485798_69485799del , CM000672.2:g.69485798_69485799del	GRCh38
NC_000010.10:g.71245554_71245555del , CM000672.1:g.71245554_71245555del	GRCh37
NC_000010.9:g.70915560_70915561del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+583_357+584del MANE Select	ENSP00000362387.2:n.357+583_357+584del
ENST00000373290.6:c.357+583_357+584del	ENSP00000362387.2:n.357+583_357+584del
ENST00000452130.1:c.84+583_84+584del	ENSP00000404528.1:n.84+583_84+584del
ENST00000475069.5:n.127+583_127+584del
NM_012339.3:c.357+583_357+584del	NP_036471.1:n.357+583_357+584del
XM_005269667.3:c.97-9796_97-9795del	XP_005269724.1:n.97-9796_97-9795del
XM_006717738.2:c.285+583_285+584del	XP_006717801.1:n.285+583_285+584del
XR_945642.1:n.487+583_487+584del
NM_001351263.1:c.97-9796_97-9795del	NP_001338192.1:n.97-9796_97-9795del
NM_012339.4:c.357+583_357+584del	NP_036471.1:n.357+583_357+584del
NR_147091.1:n.485+583_485+584del
XM_017016010.1:c.357+583_357+584del	XP_016871499.1:n.357+583_357+584del
XR_001747072.1:n.488+583_488+584del
XR_001747073.1:n.488+583_488+584del
XR_001747074.1:n.485+583_485+584del
NM_012339.5:c.357+583_357+584del MANE Select	NP_036471.1:n.357+583_357+584del
NM_001351263.2:c.97-9796_97-9795del	NP_001338192.1:n.97-9796_97-9795del
NR_147091.2:n.487+583_487+584del