Canonical Allele Identifier: CA2202023790
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2071896_2071909delinsTCCCTGCTCTTCCG , CM000678.2:g.2071896_2071909delinsTCCCTGCTCTTCCG GRCh38
NC_000016.9:g.2121897_2121910delinsTCCCTGCTCTTCCG , CM000678.1:g.2121897_2121910delinsTCCCTGCTCTTCCG GRCh37
NC_000016.8:g.2061898_2061911delinsTCCCTGCTCTTCCG NCBI36
NG_005895.1:g.27591_27604delinsTCCCTGCTCTTCCG , LRG_487:g.27591_27604delinsTCCCTGCTCTTCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*606_*619delinsTCCCTGCTCTTCCG ENSP00000455997.2:n.*606_*619delinsTCCCTG...
ENST00000642206.2:c.2104_2117delinsTCCCTGCTCTTCCG ENSP00000495146.2:p.Ser702=
ENST00000642365.2:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000495459.2:p.Ser687=
ENST00000644417.2:c.*1496_*1509delinsTCCCTGCTCTTCCG ENSP00000493912.2:n.*1496_*1509delinsTCCC...
ENST00000646464.2:c.*1664_*1677delinsTCCCTGCTCTTCCG ENSP00000496610.2:n.*1664_*1677delinsTCCC...
ENST00000219476.9:c.2059_2072delinsTCCCTGCTCTTCCG MANE Select ENSP00000219476.3:p.Ser687=
ENST00000350773.9:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000344383.4:p.Ser687=
ENST00000401874.7:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000384468.2:p.Ser687=
ENST00000563346.2:n.237_250delinsTCCCTGCTCTTCCG
ENST00000568454.6:c.2092_2105delinsTCCCTGCTCTTCCG ENSP00000454487.1:p.Ser698=
ENST00000642365.1:c.716_729delinsTCCCTGCTCTTCCG
ENST00000642561.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000495099.1:p.Ser687=
ENST00000642797.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000493846.1:p.Ser687=
ENST00000642936.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000494514.1:p.Ser687=
ENST00000643088.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000494747.1:p.Ser687=
ENST00000643298.1:c.*1561_*1574delinsTCCCTGCTCTTCCG ENSP00000494393.1:n.*1561_*1574delinsTCCC...
ENST00000643946.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000495927.1:p.Ser687=
ENST00000644043.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000496262.1:p.Ser687=
ENST00000644329.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000496611.1:p.Ser687=
ENST00000644335.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000496317.1:p.Ser687=
ENST00000644399.1:c.2052_2065delinsTCCCTGCTCTTCCG
ENST00000644847.1:n.1051_1064delinsTCCCTGCTCTTCCG
ENST00000645024.1:n.341_354delinsTCCCTGCTCTTCCG
ENST00000645552.1:n.339_352delinsTCCCTGCTCTTCCG
ENST00000646388.1:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000495921.1:p.Ser687=
ENST00000646464.1:c.112_125delinsTCCCTGCTCTTCCG ENSP00000496610.1:p.Ser38=
ENST00000646634.1:n.1072_1085delinsTCCCTGCTCTTCCG
ENST00000219476.7:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000219476.3:p.Ser687=
ENST00000350773.8:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000344383.4:p.Ser687=
ENST00000382538.10:c.1912_1925delinsTCCCTGCTCTTCCG ENSP00000371978.6:p.Ser638=
ENST00000401874.6:c.2059_2072delinsTCCCTGCTCTTCCG ENSP00000384468.2:p.Ser687=
ENST00000439117.6:c.*1358_*1371delinsTCCCTGCTCTTCCG ENSP00000406980.2:n.*1358_*1371delinsTCCC...
ENST00000439673.6:c.1948_1961delinsTCCCTGCTCTTCCG ENSP00000399232.2:p.Ser650=
ENST00000563346.1:n.128_141delinsTCCCTGCTCTTCCG
ENST00000568454.5:c.2092_2105delinsTCCCTGCTCTTCCG ENSP00000454487.1:p.Ser698=
NM_000548.3:c.2059_2072delinsTCCCTGCTCTTCCG , LRG_487t1:c.2059_2072delinsTCCCTGCTCTTCCG NP_000539.2:p.Ser687=
NM_001077183.1:c.2059_2072delinsTCCCTGCTCTTCCG NP_001070651.1:p.Ser687=
NM_001114382.1:c.2059_2072delinsTCCCTGCTCTTCCG NP_001107854.1:p.Ser687=
XM_005255529.3:c.2059_2072delinsTCCCTGCTCTTCCG XP_005255586.2:p.Ser687=
XM_005255531.3:c.2059_2072delinsTCCCTGCTCTTCCG XP_005255588.2:p.Ser687=
XM_011522636.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520938.1:p.Ser687=
XM_011522637.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520939.1:p.Ser687=
XM_011522638.1:c.1948_1961delinsTCCCTGCTCTTCCG XP_011520940.1:p.Ser650=
XM_011522639.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520941.1:p.Ser687=
XM_011522640.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520942.1:p.Ser687=
XM_011522641.1:c.1948_1961delinsTCCCTGCTCTTCCG XP_011520943.1:p.Ser650=
NM_000548.4:c.2059_2072delinsTCCCTGCTCTTCCG NP_000539.2:p.Ser687=
NM_001077183.2:c.2059_2072delinsTCCCTGCTCTTCCG NP_001070651.1:p.Ser687=
NM_001114382.2:c.2059_2072delinsTCCCTGCTCTTCCG NP_001107854.1:p.Ser687=
NM_001318827.1:c.1948_1961delinsTCCCTGCTCTTCCG NP_001305756.1:p.Ser650=
NM_001318829.1:c.1912_1925delinsTCCCTGCTCTTCCG NP_001305758.1:p.Ser638=
NM_001318831.1:c.1459_1472delinsTCCCTGCTCTTCCG NP_001305760.1:p.Ser487=
NM_001318832.1:c.2092_2105delinsTCCCTGCTCTTCCG NP_001305761.1:p.Ser698=
NM_001363528.1:c.2059_2072delinsTCCCTGCTCTTCCG NP_001350457.1:p.Ser687=
NM_021055.2:c.2059_2072delinsTCCCTGCTCTTCCG NP_066399.2:p.Ser687=
XM_005255531.4:c.2059_2072delinsTCCCTGCTCTTCCG XP_005255588.2:p.Ser687=
XM_011522636.2:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520938.1:p.Ser687=
XM_011522637.2:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520939.1:p.Ser687=
XM_011522638.2:c.2221_2234delinsTCCCTGCTCTTCCG XP_011520940.2:p.Ser741=
XM_011522639.2:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520941.1:p.Ser687=
XM_011522640.2:c.2059_2072delinsTCCCTGCTCTTCCG XP_011520942.1:p.Ser687=
XM_017023615.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_016879104.1:p.Ser687=
XM_017023616.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_016879105.1:p.Ser687=
XM_017023617.1:c.2221_2234delinsTCCCTGCTCTTCCG XP_016879106.1:p.Ser741=
XM_017023618.1:c.715_728delinsTCCCTGCTCTTCCG XP_016879107.1:p.Ser239=
XM_024450413.1:c.2059_2072delinsTCCCTGCTCTTCCG XP_024306181.1:p.Ser687=
NM_000548.5:c.2059_2072delinsTCCCTGCTCTTCCG MANE Select NP_000539.2:p.Ser687=
NM_001370404.1:c.2059_2072delinsTCCCTGCTCTTCCG NP_001357333.1:p.Ser687=
NM_001370405.1:c.2059_2072delinsTCCCTGCTCTTCCG NP_001357334.1:p.Ser687=
NM_001077183.3:c.2059_2072delinsTCCCTGCTCTTCCG NP_001070651.1:p.Ser687=
NM_001114382.3:c.2059_2072delinsTCCCTGCTCTTCCG NP_001107854.1:p.Ser687=
NM_001318827.2:c.1948_1961delinsTCCCTGCTCTTCCG NP_001305756.1:p.Ser650=
NM_001318829.2:c.1912_1925delinsTCCCTGCTCTTCCG NP_001305758.1:p.Ser638=
NM_001318831.2:c.1459_1472delinsTCCCTGCTCTTCCG NP_001305760.1:p.Ser487=
NM_001318832.2:c.2092_2105delinsTCCCTGCTCTTCCG NP_001305761.1:p.Ser698=
NM_001363528.2:c.2059_2072delinsTCCCTGCTCTTCCG NP_001350457.1:p.Ser687=
NM_021055.3:c.2059_2072delinsTCCCTGCTCTTCCG NP_066399.2:p.Ser687=