Canonical Allele Identifier: CA2788417229

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503534del , CM000672.2:g.69503534del	GRCh38
NC_000010.10:g.71263290del , CM000672.1:g.71263290del	GRCh37
NC_000010.9:g.70933296del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.571-904del MANE Select	ENSP00000362387.2:n.571-904del
ENST00000373290.6:c.571-904del	ENSP00000362387.2:n.571-904del
ENST00000452130.1:c.298-904del	ENSP00000404528.1:n.298-904del
ENST00000459981.1:n.503-904del
ENST00000475069.5:n.341-904del
ENST00000486093.5:n.280-904del
ENST00000490083.5:n.517-904del
NM_012339.3:c.571-904del	NP_036471.1:n.571-904del
XM_005269666.3:c.376-904del	XP_005269723.1:n.376-904del
XM_005269667.3:c.310-904del	XP_005269724.1:n.310-904del
XM_006717738.2:c.499-904del	XP_006717801.1:n.499-904del
XM_011539562.1:c.223-904del	XP_011537864.1:n.223-904del
XM_011539563.1:c.139-904del	XP_011537865.1:n.139-904del
XR_945642.1:n.772-904del
NM_001351263.1:c.310-904del	NP_001338192.1:n.310-904del
NM_012339.4:c.571-904del	NP_036471.1:n.571-904del
NR_147091.1:n.770-904del
XM_005269666.4:c.376-904del	XP_005269723.1:n.376-904del
XM_011539562.2:c.223-904del	XP_011537864.1:n.223-904del
XM_011539563.2:c.139-904del	XP_011537865.1:n.139-904del
XM_017016010.1:c.642-904del	XP_016871499.1:n.642-904del
XR_001747072.1:n.773-904del
XR_001747073.1:n.773-904del
XR_001747074.1:n.699-904del
NM_012339.5:c.571-904del MANE Select	NP_036471.1:n.571-904del
NM_001351263.2:c.310-904del	NP_001338192.1:n.310-904del
NR_147091.2:n.772-904del