Canonical Allele Identifier: CA209260812

Gene: TSPAN15

Linked Data

• dbSNP Id: rs764035862
• gnomAD v4: 10-69485338-GA-G
• MyVariant Identifiers: chr10:g.71245095del (hg19) ; chr10:g.69485339del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485341del , CM000672.2:g.69485341del	GRCh38
NC_000010.10:g.71245097del , CM000672.1:g.71245097del	GRCh37
NC_000010.9:g.70915103del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+126del MANE Select	ENSP00000362387.2:n.357+126del
ENST00000373290.6:c.357+126del	ENSP00000362387.2:n.357+126del
ENST00000452130.1:c.84+126del	ENSP00000404528.1:n.84+126del
ENST00000475069.5:n.127+126del
NM_012339.3:c.357+126del	NP_036471.1:n.357+126del
XM_005269667.3:c.97-10253del	XP_005269724.1:n.97-10253del
XM_006717738.2:c.285+126del	XP_006717801.1:n.285+126del
XR_945642.1:n.487+126del
NM_001351263.1:c.97-10253del	NP_001338192.1:n.97-10253del
NM_012339.4:c.357+126del	NP_036471.1:n.357+126del
NR_147091.1:n.485+126del
XM_017016010.1:c.357+126del	XP_016871499.1:n.357+126del
XR_001747072.1:n.488+126del
XR_001747073.1:n.488+126del
XR_001747074.1:n.485+126del
NM_012339.5:c.357+126del MANE Select	NP_036471.1:n.357+126del
NM_001351263.2:c.97-10253del	NP_001338192.1:n.97-10253del
NR_147091.2:n.487+126del