Canonical Allele Identifier: CA1917825949

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1842253453

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503551del , CM000672.2:g.69503551del	GRCh38
NC_000010.10:g.71263307del , CM000672.1:g.71263307del	GRCh37
NC_000010.9:g.70933313del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.571-887del MANE Select	ENSP00000362387.2:n.571-887del
ENST00000373290.6:c.571-887del	ENSP00000362387.2:n.571-887del
ENST00000452130.1:c.298-887del	ENSP00000404528.1:n.298-887del
ENST00000459981.1:n.503-887del
ENST00000475069.5:n.341-887del
ENST00000486093.5:n.280-887del
ENST00000490083.5:n.517-887del
NM_012339.3:c.571-887del	NP_036471.1:n.571-887del
XM_005269666.3:c.376-887del	XP_005269723.1:n.376-887del
XM_005269667.3:c.310-887del	XP_005269724.1:n.310-887del
XM_006717738.2:c.499-887del	XP_006717801.1:n.499-887del
XM_011539562.1:c.223-887del	XP_011537864.1:n.223-887del
XM_011539563.1:c.139-887del	XP_011537865.1:n.139-887del
XR_945642.1:n.772-887del
NM_001351263.1:c.310-887del	NP_001338192.1:n.310-887del
NM_012339.4:c.571-887del	NP_036471.1:n.571-887del
NR_147091.1:n.770-887del
XM_005269666.4:c.376-887del	XP_005269723.1:n.376-887del
XM_011539562.2:c.223-887del	XP_011537864.1:n.223-887del
XM_011539563.2:c.139-887del	XP_011537865.1:n.139-887del
XM_017016010.1:c.642-887del	XP_016871499.1:n.642-887del
XR_001747072.1:n.773-887del
XR_001747073.1:n.773-887del
XR_001747074.1:n.699-887del
NM_012339.5:c.571-887del MANE Select	NP_036471.1:n.571-887del
NM_001351263.2:c.310-887del	NP_001338192.1:n.310-887del
NR_147091.2:n.772-887del