Canonical Allele Identifier: CA2788417226

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503441_69503444dup , CM000672.2:g.69503441_69503444dup	GRCh38
NC_000010.10:g.71263197_71263200dup , CM000672.1:g.71263197_71263200dup	GRCh37
NC_000010.9:g.70933203_70933206dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.571-997_571-994dup MANE Select	ENSP00000362387.2:n.571-997_571-994dup
ENST00000373290.6:c.571-997_571-994dup	ENSP00000362387.2:n.571-997_571-994dup
ENST00000452130.1:c.298-997_298-994dup	ENSP00000404528.1:n.298-997_298-994dup
ENST00000459981.1:n.503-997_503-994dup
ENST00000475069.5:n.341-997_341-994dup
ENST00000486093.5:n.280-997_280-994dup
ENST00000490083.5:n.517-997_517-994dup
NM_012339.3:c.571-997_571-994dup	NP_036471.1:n.571-997_571-994dup
XM_005269666.3:c.376-997_376-994dup	XP_005269723.1:n.376-997_376-994dup
XM_005269667.3:c.310-997_310-994dup	XP_005269724.1:n.310-997_310-994dup
XM_006717738.2:c.499-997_499-994dup	XP_006717801.1:n.499-997_499-994dup
XM_011539562.1:c.223-997_223-994dup	XP_011537864.1:n.223-997_223-994dup
XM_011539563.1:c.139-997_139-994dup	XP_011537865.1:n.139-997_139-994dup
XR_945642.1:n.772-997_772-994dup
NM_001351263.1:c.310-997_310-994dup	NP_001338192.1:n.310-997_310-994dup
NM_012339.4:c.571-997_571-994dup	NP_036471.1:n.571-997_571-994dup
NR_147091.1:n.770-997_770-994dup
XM_005269666.4:c.376-997_376-994dup	XP_005269723.1:n.376-997_376-994dup
XM_011539562.2:c.223-997_223-994dup	XP_011537864.1:n.223-997_223-994dup
XM_011539563.2:c.139-997_139-994dup	XP_011537865.1:n.139-997_139-994dup
XM_017016010.1:c.642-997_642-994dup	XP_016871499.1:n.642-997_642-994dup
XR_001747072.1:n.773-997_773-994dup
XR_001747073.1:n.773-997_773-994dup
XR_001747074.1:n.699-997_699-994dup
NM_012339.5:c.571-997_571-994dup MANE Select	NP_036471.1:n.571-997_571-994dup
NM_001351263.2:c.310-997_310-994dup	NP_001338192.1:n.310-997_310-994dup
NR_147091.2:n.772-997_772-994dup