Canonical Allele Identifier: CA658656500
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448727
ClinVar RCV Id: RCV000517463
dbSNP Id: rs1555510519

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2079308del , CM000678.2:g.2079308del GRCh38
NC_000016.9:g.2129309del , CM000678.1:g.2129309del GRCh37
NC_000016.8:g.2069310del NCBI36
NG_005895.1:g.35003del , LRG_487:g.35003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*1582del ENSP00000455997.2:n.*1582del
ENST00000642206.2:c.3080del ENSP00000495146.2:p.Gly1027AlafsTer15
ENST00000642365.2:c.3161del ENSP00000495459.2:p.Gly1054AlafsTer15
ENST00000644417.2:c.*3613del ENSP00000493912.2:n.*3613del
ENST00000646464.2:c.*4086del ENSP00000496610.2:n.*4086del
ENST00000219476.9:c.3164del MANE Select ENSP00000219476.3:p.Gly1055AlafsTer15
ENST00000350773.9:c.3164del ENSP00000344383.4:p.Gly1055AlafsTer15
ENST00000401874.7:c.3032del ENSP00000384468.2:p.Gly1011AlafsTer15
ENST00000471143.6:c.392del ENSP00000458541.2:n.392del
ENST00000568366.6:n.521del
ENST00000568454.6:c.3065del ENSP00000454487.1:p.Gly1022AlafsTer15
ENST00000642365.1:c.1818del
ENST00000642561.1:c.3035del ENSP00000495099.1:p.Gly1012AlafsTer15
ENST00000642797.1:c.3035del ENSP00000493846.1:p.Gly1012AlafsTer15
ENST00000642936.1:c.3032del ENSP00000494514.1:p.Gly1011AlafsTer15
ENST00000643088.1:c.3032del ENSP00000494747.1:p.Gly1011AlafsTer15
ENST00000643946.1:c.3164del ENSP00000495927.1:p.Gly1055AlafsTer15
ENST00000644043.1:c.3035del ENSP00000496262.1:p.Gly1012AlafsTer15
ENST00000644329.1:c.3032del ENSP00000496611.1:p.Gly1011AlafsTer15
ENST00000644335.1:c.3035del ENSP00000496317.1:p.Gly1012AlafsTer15
ENST00000644399.1:c.3154del
ENST00000644722.1:n.310del
ENST00000645024.1:n.1317del
ENST00000646388.1:c.3164del ENSP00000495921.1:p.Gly1055AlafsTer15
ENST00000646634.1:n.2048del
ENST00000647042.1:n.456del
ENST00000219476.7:c.3164del ENSP00000219476.3:p.Gly1055AlafsTer15
ENST00000350773.8:c.3164del ENSP00000344383.4:p.Gly1055AlafsTer15
ENST00000382538.10:c.2888del ENSP00000371978.6:p.Gly963AlafsTer15
ENST00000401874.6:c.3032del ENSP00000384468.2:p.Gly1011AlafsTer15
ENST00000439117.6:c.*2331del ENSP00000406980.2:n.*2331del
ENST00000439673.6:c.2924del ENSP00000399232.2:p.Gly975AlafsTer15
ENST00000471143.5:c.390del
ENST00000483020.5:c.404del ENSP00000460310.1:n.404del
ENST00000497886.5:n.991del
ENST00000561695.1:n.389del
ENST00000568366.5:n.521del
ENST00000568454.5:c.3065del ENSP00000454487.1:p.Gly1022AlafsTer15
NM_000548.3:c.3164del , LRG_487t1:c.3164del NP_000539.2:p.Gly1055AlafsTer15
NM_001077183.1:c.3032del NP_001070651.1:p.Gly1011AlafsTer15
NM_001114382.1:c.3164del NP_001107854.1:p.Gly1055AlafsTer15
XM_005255529.3:c.3035del XP_005255586.2:p.Gly1012AlafsTer15
XM_005255531.3:c.3035del XP_005255588.2:p.Gly1012AlafsTer15
XM_011522636.1:c.3164del XP_011520938.1:p.Gly1055AlafsTer15
XM_011522637.1:c.3161del XP_011520939.1:p.Gly1054AlafsTer15
XM_011522638.1:c.3053del XP_011520940.1:p.Gly1018AlafsTer15
XM_011522639.1:c.3035del XP_011520941.1:p.Gly1012AlafsTer15
XM_011522640.1:c.3032del XP_011520942.1:p.Gly1011AlafsTer15
XM_011522641.1:c.2924del XP_011520943.1:p.Gly975AlafsTer15
NM_000548.4:c.3164del NP_000539.2:p.Gly1055AlafsTer15
NM_001077183.2:c.3032del NP_001070651.1:p.Gly1011AlafsTer15
NM_001114382.2:c.3164del NP_001107854.1:p.Gly1055AlafsTer15
NM_001318827.1:c.2924del NP_001305756.1:p.Gly975AlafsTer15
NM_001318829.1:c.2888del NP_001305758.1:p.Gly963AlafsTer15
NM_001318831.1:c.2432del NP_001305760.1:p.Gly811AlafsTer15
NM_001318832.1:c.3065del NP_001305761.1:p.Gly1022AlafsTer15
NM_001363528.1:c.3035del NP_001350457.1:p.Gly1012AlafsTer15
NM_021055.2:c.3035del NP_066399.2:p.Gly1012AlafsTer15
XM_005255531.4:c.3035del XP_005255588.2:p.Gly1012AlafsTer15
XM_011522636.2:c.3164del XP_011520938.1:p.Gly1055AlafsTer15
XM_011522637.2:c.3161del XP_011520939.1:p.Gly1054AlafsTer15
XM_011522638.2:c.3326del XP_011520940.2:p.Gly1109AlafsTer15
XM_011522639.2:c.3035del XP_011520941.1:p.Gly1012AlafsTer15
XM_011522640.2:c.3032del XP_011520942.1:p.Gly1011AlafsTer15
XM_017023615.1:c.3161del XP_016879104.1:p.Gly1054AlafsTer15
XM_017023616.1:c.3032del XP_016879105.1:p.Gly1011AlafsTer15
XM_017023617.1:c.3197del XP_016879106.1:p.Gly1066AlafsTer15
XM_017023618.1:c.1820del XP_016879107.1:p.Gly607AlafsTer15
XM_024450413.1:c.3032del XP_024306181.1:p.Gly1011AlafsTer15
NM_000548.5:c.3164del MANE Select NP_000539.2:p.Gly1055AlafsTer15
NM_001370404.1:c.3032del NP_001357333.1:p.Gly1011AlafsTer15
NM_001370405.1:c.3035del NP_001357334.1:p.Gly1012AlafsTer15
NM_001077183.3:c.3032del NP_001070651.1:p.Gly1011AlafsTer15
NM_001114382.3:c.3164del NP_001107854.1:p.Gly1055AlafsTer15
NM_001318827.2:c.2924del NP_001305756.1:p.Gly975AlafsTer15
NM_001318829.2:c.2888del NP_001305758.1:p.Gly963AlafsTer15
NM_001318831.2:c.2432del NP_001305760.1:p.Gly811AlafsTer15
NM_001318832.2:c.3065del NP_001305761.1:p.Gly1022AlafsTer15
NM_001363528.2:c.3035del NP_001350457.1:p.Gly1012AlafsTer15
NM_021055.3:c.3035del NP_066399.2:p.Gly1012AlafsTer15