Canonical Allele Identifier: CA1917825905

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503440_69503441delinsTG , CM000672.2:g.69503440_69503441delinsTG	GRCh38
NC_000010.10:g.71263196_71263197delinsTG , CM000672.1:g.71263196_71263197delinsTG	GRCh37
NC_000010.9:g.70933202_70933203delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.571-998_571-997delinsTG MANE Select	ENSP00000362387.2:n.571-998_571-997delins...
ENST00000373290.6:c.571-998_571-997delinsTG	ENSP00000362387.2:n.571-998_571-997delins...
ENST00000452130.1:c.298-998_298-997delinsTG	ENSP00000404528.1:n.298-998_298-997delins...
ENST00000459981.1:n.503-998_503-997delinsTG
ENST00000475069.5:n.341-998_341-997delinsTG
ENST00000486093.5:n.280-998_280-997delinsTG
ENST00000490083.5:n.517-998_517-997delinsTG
NM_012339.3:c.571-998_571-997delinsTG	NP_036471.1:n.571-998_571-997delinsTG
XM_005269666.3:c.376-998_376-997delinsTG	XP_005269723.1:n.376-998_376-997delinsTG
XM_005269667.3:c.310-998_310-997delinsTG	XP_005269724.1:n.310-998_310-997delinsTG
XM_006717738.2:c.499-998_499-997delinsTG	XP_006717801.1:n.499-998_499-997delinsTG
XM_011539562.1:c.223-998_223-997delinsTG	XP_011537864.1:n.223-998_223-997delinsTG
XM_011539563.1:c.139-998_139-997delinsTG	XP_011537865.1:n.139-998_139-997delinsTG
XR_945642.1:n.772-998_772-997delinsTG
NM_001351263.1:c.310-998_310-997delinsTG	NP_001338192.1:n.310-998_310-997delinsTG
NM_012339.4:c.571-998_571-997delinsTG	NP_036471.1:n.571-998_571-997delinsTG
NR_147091.1:n.770-998_770-997delinsTG
XM_005269666.4:c.376-998_376-997delinsTG	XP_005269723.1:n.376-998_376-997delinsTG
XM_011539562.2:c.223-998_223-997delinsTG	XP_011537864.1:n.223-998_223-997delinsTG
XM_011539563.2:c.139-998_139-997delinsTG	XP_011537865.1:n.139-998_139-997delinsTG
XM_017016010.1:c.642-998_642-997delinsTG	XP_016871499.1:n.642-998_642-997delinsTG
XR_001747072.1:n.773-998_773-997delinsTG
XR_001747073.1:n.773-998_773-997delinsTG
XR_001747074.1:n.699-998_699-997delinsTG
NM_012339.5:c.571-998_571-997delinsTG MANE Select	NP_036471.1:n.571-998_571-997delinsTG
NM_001351263.2:c.310-998_310-997delinsTG	NP_001338192.1:n.310-998_310-997delinsTG
NR_147091.2:n.772-998_772-997delinsTG