Canonical Allele Identifier: CA929627171

Gene: TSPAN15

Linked Data

• gnomAD v3: 10-69485861-A-AGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
• gnomAD v4: 10-69485861-A-AGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485861_69485862insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG , CM000672.2:g.69485861_69485862insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	GRCh38
NC_000010.10:g.71245617_71245618insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG , CM000672.1:g.71245617_71245618insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	GRCh37
NC_000010.9:g.70915623_70915624insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG MANE Select	ENSP00000362387.2:n.357+646_357+647insGGCAGTACCATCAGAGGCTGTAA...
ENST00000373290.6:c.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	ENSP00000362387.2:n.357+646_357+647insGGCAGTACCATCAGAGGCTGTAA...
ENST00000452130.1:c.84+646_84+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	ENSP00000404528.1:n.84+646_84+647insGGCAGTACCATCAGAGGCTGTAAAA...
ENST00000475069.5:n.127+646_127+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
NM_012339.3:c.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	NP_036471.1:n.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATA...
XM_005269667.3:c.97-9733_97-9732insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	XP_005269724.1:n.97-9733_97-9732insGGCAGTACCATCAGAGGCTGTAAAAC...
XM_006717738.2:c.285+646_285+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	XP_006717801.1:n.285+646_285+647insGGCAGTACCATCAGAGGCTGTAAAAC...
XR_945642.1:n.487+646_487+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
NM_001351263.1:c.97-9733_97-9732insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	NP_001338192.1:n.97-9733_97-9732insGGCAGTACCATCAGAGGCTGTAAAAC...
NM_012339.4:c.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	NP_036471.1:n.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATA...
NR_147091.1:n.485+646_485+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
XM_017016010.1:c.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	XP_016871499.1:n.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAAC...
XR_001747072.1:n.488+646_488+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
XR_001747073.1:n.488+646_488+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
XR_001747074.1:n.485+646_485+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG
NM_012339.5:c.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG MANE Select	NP_036471.1:n.357+646_357+647insGGCAGTACCATCAGAGGCTGTAAAACATA...
NM_001351263.2:c.97-9733_97-9732insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG	NP_001338192.1:n.97-9733_97-9732insGGCAGTACCATCAGAGGCTGTAAAAC...
NR_147091.2:n.487+646_487+647insGGCAGTACCATCAGAGGCTGTAAAACATACATCAAATCGCCTTTATG