Canonical Allele Identifier: CA1917825918

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503479_69503481delinsTTC , CM000672.2:g.69503479_69503481delinsTTC	GRCh38
NC_000010.10:g.71263235_71263237delinsTTC , CM000672.1:g.71263235_71263237delinsTTC	GRCh37
NC_000010.9:g.70933241_70933243delinsTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.571-959_571-957delinsTTC MANE Select	ENSP00000362387.2:n.571-959_571-957delinsTTC
ENST00000373290.6:c.571-959_571-957delinsTTC	ENSP00000362387.2:n.571-959_571-957delinsTTC
ENST00000452130.1:c.298-959_298-957delinsTTC	ENSP00000404528.1:n.298-959_298-957delinsTTC
ENST00000459981.1:n.503-959_503-957delinsTTC
ENST00000475069.5:n.341-959_341-957delinsTTC
ENST00000486093.5:n.280-959_280-957delinsTTC
ENST00000490083.5:n.517-959_517-957delinsTTC
NM_012339.3:c.571-959_571-957delinsTTC	NP_036471.1:n.571-959_571-957delinsTTC
XM_005269666.3:c.376-959_376-957delinsTTC	XP_005269723.1:n.376-959_376-957delinsTTC
XM_005269667.3:c.310-959_310-957delinsTTC	XP_005269724.1:n.310-959_310-957delinsTTC
XM_006717738.2:c.499-959_499-957delinsTTC	XP_006717801.1:n.499-959_499-957delinsTTC
XM_011539562.1:c.223-959_223-957delinsTTC	XP_011537864.1:n.223-959_223-957delinsTTC
XM_011539563.1:c.139-959_139-957delinsTTC	XP_011537865.1:n.139-959_139-957delinsTTC
XR_945642.1:n.772-959_772-957delinsTTC
NM_001351263.1:c.310-959_310-957delinsTTC	NP_001338192.1:n.310-959_310-957delinsTTC
NM_012339.4:c.571-959_571-957delinsTTC	NP_036471.1:n.571-959_571-957delinsTTC
NR_147091.1:n.770-959_770-957delinsTTC
XM_005269666.4:c.376-959_376-957delinsTTC	XP_005269723.1:n.376-959_376-957delinsTTC
XM_011539562.2:c.223-959_223-957delinsTTC	XP_011537864.1:n.223-959_223-957delinsTTC
XM_011539563.2:c.139-959_139-957delinsTTC	XP_011537865.1:n.139-959_139-957delinsTTC
XM_017016010.1:c.642-959_642-957delinsTTC	XP_016871499.1:n.642-959_642-957delinsTTC
XR_001747072.1:n.773-959_773-957delinsTTC
XR_001747073.1:n.773-959_773-957delinsTTC
XR_001747074.1:n.699-959_699-957delinsTTC
NM_012339.5:c.571-959_571-957delinsTTC MANE Select	NP_036471.1:n.571-959_571-957delinsTTC
NM_001351263.2:c.310-959_310-957delinsTTC	NP_001338192.1:n.310-959_310-957delinsTTC
NR_147091.2:n.772-959_772-957delinsTTC