Canonical Allele Identifier: CA2609454740

Gene: TSPAN15

Linked Data

• gnomAD v4: 10-69485332-T-TCAGCTTGGTTCATTTTCTTAGTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485333_69485334insAGCTTGGTTCATTTTCTTAGTCGC , CM000672.2:g.69485333_69485334insAGCTTGGTTCATTTTCTTAGTCGC	GRCh38
NC_000010.10:g.71245089_71245090insAGCTTGGTTCATTTTCTTAGTCGC , CM000672.1:g.71245089_71245090insAGCTTGGTTCATTTTCTTAGTCGC	GRCh37
NC_000010.9:g.70915095_70915096insAGCTTGGTTCATTTTCTTAGTCGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC MANE Select	ENSP00000362387.2:n.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCG...
ENST00000373290.6:c.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC	ENSP00000362387.2:n.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCG...
ENST00000452130.1:c.84+118_84+119insAGCTTGGTTCATTTTCTTAGTCGC	ENSP00000404528.1:n.84+118_84+119insAGCTTGGTTCATTTTCTTAGTCGC
ENST00000475069.5:n.127+118_127+119insAGCTTGGTTCATTTTCTTAGTCGC
NM_012339.3:c.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC	NP_036471.1:n.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC
XM_005269667.3:c.97-10261_97-10260insAGCTTGGTTCATTTTCTTAGTCGC	XP_005269724.1:n.97-10261_97-10260insAGCTTGGTTCATTTTCTTAGTCGC...
XM_006717738.2:c.285+118_285+119insAGCTTGGTTCATTTTCTTAGTCGC	XP_006717801.1:n.285+118_285+119insAGCTTGGTTCATTTTCTTAGTCGC
XR_945642.1:n.487+118_487+119insAGCTTGGTTCATTTTCTTAGTCGC
NM_001351263.1:c.97-10261_97-10260insAGCTTGGTTCATTTTCTTAGTCGC	NP_001338192.1:n.97-10261_97-10260insAGCTTGGTTCATTTTCTTAGTCGC...
NM_012339.4:c.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC	NP_036471.1:n.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC
NR_147091.1:n.485+118_485+119insAGCTTGGTTCATTTTCTTAGTCGC
XM_017016010.1:c.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC	XP_016871499.1:n.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC
XR_001747072.1:n.488+118_488+119insAGCTTGGTTCATTTTCTTAGTCGC
XR_001747073.1:n.488+118_488+119insAGCTTGGTTCATTTTCTTAGTCGC
XR_001747074.1:n.485+118_485+119insAGCTTGGTTCATTTTCTTAGTCGC
NM_012339.5:c.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC MANE Select	NP_036471.1:n.357+118_357+119insAGCTTGGTTCATTTTCTTAGTCGC
NM_001351263.2:c.97-10261_97-10260insAGCTTGGTTCATTTTCTTAGTCGC	NP_001338192.1:n.97-10261_97-10260insAGCTTGGTTCATTTTCTTAGTCGC...
NR_147091.2:n.487+118_487+119insAGCTTGGTTCATTTTCTTAGTCGC