Canonical Allele Identifier: CA918700621

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1589642670

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485844_69485847del , CM000672.2:g.69485844_69485847del	GRCh38
NC_000010.10:g.71245600_71245603del , CM000672.1:g.71245600_71245603del	GRCh37
NC_000010.9:g.70915606_70915609del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+629_357+632del MANE Select	ENSP00000362387.2:n.357+629_357+632del
ENST00000373290.6:c.357+629_357+632del	ENSP00000362387.2:n.357+629_357+632del
ENST00000452130.1:c.84+629_84+632del	ENSP00000404528.1:n.84+629_84+632del
ENST00000475069.5:n.127+629_127+632del
NM_012339.3:c.357+629_357+632del	NP_036471.1:n.357+629_357+632del
XM_005269667.3:c.97-9750_97-9747del	XP_005269724.1:n.97-9750_97-9747del
XM_006717738.2:c.285+629_285+632del	XP_006717801.1:n.285+629_285+632del
XR_945642.1:n.487+629_487+632del
NM_001351263.1:c.97-9750_97-9747del	NP_001338192.1:n.97-9750_97-9747del
NM_012339.4:c.357+629_357+632del	NP_036471.1:n.357+629_357+632del
NR_147091.1:n.485+629_485+632del
XM_017016010.1:c.357+629_357+632del	XP_016871499.1:n.357+629_357+632del
XR_001747072.1:n.488+629_488+632del
XR_001747073.1:n.488+629_488+632del
XR_001747074.1:n.485+629_485+632del
NM_012339.5:c.357+629_357+632del MANE Select	NP_036471.1:n.357+629_357+632del
NM_001351263.2:c.97-9750_97-9747del	NP_001338192.1:n.97-9750_97-9747del
NR_147091.2:n.487+629_487+632del