Canonical Allele Identifier: CA1917825948

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503550_69503551delinsCT , CM000672.2:g.69503550_69503551delinsCT	GRCh38
NC_000010.10:g.71263306_71263307delinsCT , CM000672.1:g.71263306_71263307delinsCT	GRCh37
NC_000010.9:g.70933312_70933313delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.571-888_571-887delinsCT MANE Select	ENSP00000362387.2:n.571-888_571-887delins...
ENST00000373290.6:c.571-888_571-887delinsCT	ENSP00000362387.2:n.571-888_571-887delins...
ENST00000452130.1:c.298-888_298-887delinsCT	ENSP00000404528.1:n.298-888_298-887delins...
ENST00000459981.1:n.503-888_503-887delinsCT
ENST00000475069.5:n.341-888_341-887delinsCT
ENST00000486093.5:n.280-888_280-887delinsCT
ENST00000490083.5:n.517-888_517-887delinsCT
NM_012339.3:c.571-888_571-887delinsCT	NP_036471.1:n.571-888_571-887delinsCT
XM_005269666.3:c.376-888_376-887delinsCT	XP_005269723.1:n.376-888_376-887delinsCT
XM_005269667.3:c.310-888_310-887delinsCT	XP_005269724.1:n.310-888_310-887delinsCT
XM_006717738.2:c.499-888_499-887delinsCT	XP_006717801.1:n.499-888_499-887delinsCT
XM_011539562.1:c.223-888_223-887delinsCT	XP_011537864.1:n.223-888_223-887delinsCT
XM_011539563.1:c.139-888_139-887delinsCT	XP_011537865.1:n.139-888_139-887delinsCT
XR_945642.1:n.772-888_772-887delinsCT
NM_001351263.1:c.310-888_310-887delinsCT	NP_001338192.1:n.310-888_310-887delinsCT
NM_012339.4:c.571-888_571-887delinsCT	NP_036471.1:n.571-888_571-887delinsCT
NR_147091.1:n.770-888_770-887delinsCT
XM_005269666.4:c.376-888_376-887delinsCT	XP_005269723.1:n.376-888_376-887delinsCT
XM_011539562.2:c.223-888_223-887delinsCT	XP_011537864.1:n.223-888_223-887delinsCT
XM_011539563.2:c.139-888_139-887delinsCT	XP_011537865.1:n.139-888_139-887delinsCT
XM_017016010.1:c.642-888_642-887delinsCT	XP_016871499.1:n.642-888_642-887delinsCT
XR_001747072.1:n.773-888_773-887delinsCT
XR_001747073.1:n.773-888_773-887delinsCT
XR_001747074.1:n.699-888_699-887delinsCT
NM_012339.5:c.571-888_571-887delinsCT MANE Select	NP_036471.1:n.571-888_571-887delinsCT
NM_001351263.2:c.310-888_310-887delinsCT	NP_001338192.1:n.310-888_310-887delinsCT
NR_147091.2:n.772-888_772-887delinsCT