Canonical Allele Identifier: CA2202031808
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088257_2088260delinsAACC , CM000678.2:g.2088257_2088260delinsAACC GRCh38
NC_000016.9:g.2138258_2138261delinsAACC , CM000678.1:g.2138258_2138261delinsAACC GRCh37
NC_000016.8:g.2078259_2078262delinsAACC NCBI36
NG_005895.1:g.43952_43955delinsAACC , LRG_487:g.43952_43955delinsAACC
NG_008617.1:g.54961_54964delinsGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3540_*3543delinsAACC ENSP00000455997.2:n.*3540_*3543delinsAACC
ENST00000642206.2:c.5038_5041delinsAACC ENSP00000495146.2:p.Asn1680=
ENST00000642365.2:c.5188_5191delinsAACC ENSP00000495459.2:p.Asn1730=
ENST00000644417.2:c.*5704_*5707delinsAACC ENSP00000493912.2:n.*5704_*5707delinsAACC
ENST00000646464.2:c.*7940_*7943delinsAACC ENSP00000496610.2:n.*7940_*7943delinsAACC
ENST00000219476.9:c.5191_5194delinsAACC MANE Select ENSP00000219476.3:p.Asn1731=
ENST00000350773.9:c.5122_5125delinsAACC ENSP00000344383.4:p.Asn1708=
ENST00000401874.7:c.4990_4993delinsAACC ENSP00000384468.2:p.Asn1664=
ENST00000568454.6:c.5023_5026delinsAACC ENSP00000454487.1:p.Asn1675=
ENST00000569110.2:c.1414_1417delinsAACC
ENST00000569930.2:n.3073_3076delinsAACC
ENST00000642365.1:c.3845_3848delinsAACC
ENST00000642561.1:c.5050_5053delinsAACC ENSP00000495099.1:p.Asn1684=
ENST00000642791.1:n.788_791delinsAACC
ENST00000642797.1:c.4993_4996delinsAACC ENSP00000493846.1:p.Asn1665=
ENST00000642936.1:c.5059_5062delinsAACC ENSP00000494514.1:p.Asn1687=
ENST00000643088.1:c.4984_4987delinsAACC ENSP00000494747.1:p.Asn1662=
ENST00000643426.1:n.2839_2842delinsAACC
ENST00000643946.1:c.5116_5119delinsAACC ENSP00000495927.1:p.Asn1706=
ENST00000644043.1:c.5062_5065delinsAACC ENSP00000496262.1:p.Asn1688=
ENST00000644329.1:c.5077_5080delinsAACC ENSP00000496611.1:p.Asn1693=
ENST00000644335.1:c.4987_4990delinsAACC ENSP00000496317.1:p.Asn1663=
ENST00000644399.1:c.5112_5115delinsAACC
ENST00000645024.1:n.3275_3278delinsAACC
ENST00000646388.1:c.5185_5188delinsAACC ENSP00000495921.1:p.Asn1729=
ENST00000646634.1:n.4006_4009delinsAACC
ENST00000646674.1:n.2443_2446delinsAACC
ENST00000647042.1:n.2414_2417delinsAACC
ENST00000647180.1:n.2304_2307delinsAACC
ENST00000219476.7:c.5191_5194delinsAACC ENSP00000219476.3:p.Asn1731=
ENST00000350773.8:c.5122_5125delinsAACC ENSP00000344383.4:p.Asn1708=
ENST00000382538.10:c.4846_4849delinsAACC ENSP00000371978.6:p.Asn1616=
ENST00000401874.6:c.4990_4993delinsAACC ENSP00000384468.2:p.Asn1664=
ENST00000439117.6:c.*4358_*4361delinsAACC ENSP00000406980.2:n.*4358_*4361delinsAACC
ENST00000439673.6:c.4882_4885delinsAACC ENSP00000399232.2:p.Asn1628=
ENST00000497886.5:n.2914_2917delinsAACC
ENST00000568454.5:c.5023_5026delinsAACC ENSP00000454487.1:p.Asn1675=
ENST00000569110.1:c.1373_1376delinsAACC
ENST00000569930.1:n.2306_2309delinsAACC
NM_000548.3:c.5191_5194delinsAACC , LRG_487t1:c.5191_5194delinsAACC NP_000539.2:p.Asn1731=
NM_001077183.1:c.4990_4993delinsAACC NP_001070651.1:p.Asn1664=
NM_001114382.1:c.5122_5125delinsAACC NP_001107854.1:p.Asn1708=
XM_005255529.3:c.5062_5065delinsAACC XP_005255586.2:p.Asn1688=
XM_005255531.3:c.4993_4996delinsAACC XP_005255588.2:p.Asn1665=
XM_011522636.1:c.5245_5248delinsAACC XP_011520938.1:p.Asn1749=
XM_011522637.1:c.5242_5245delinsAACC XP_011520939.1:p.Asn1748=
XM_011522638.1:c.5134_5137delinsAACC XP_011520940.1:p.Asn1712=
XM_011522639.1:c.5116_5119delinsAACC XP_011520941.1:p.Asn1706=
XM_011522640.1:c.5113_5116delinsAACC XP_011520942.1:p.Asn1705=
XM_011522641.1:c.4882_4885delinsAACC XP_011520943.1:p.Asn1628=
NM_000548.4:c.5191_5194delinsAACC NP_000539.2:p.Asn1731=
NM_001077183.2:c.4990_4993delinsAACC NP_001070651.1:p.Asn1664=
NM_001114382.2:c.5122_5125delinsAACC NP_001107854.1:p.Asn1708=
NM_001318827.1:c.4882_4885delinsAACC NP_001305756.1:p.Asn1628=
NM_001318829.1:c.4846_4849delinsAACC NP_001305758.1:p.Asn1616=
NM_001318831.1:c.4459_4462delinsAACC NP_001305760.1:p.Asn1487=
NM_001318832.1:c.5023_5026delinsAACC NP_001305761.1:p.Asn1675=
NM_001363528.1:c.4993_4996delinsAACC NP_001350457.1:p.Asn1665=
NM_021055.2:c.5062_5065delinsAACC NP_066399.2:p.Asn1688=
XM_005255531.4:c.4993_4996delinsAACC XP_005255588.2:p.Asn1665=
XM_011522636.2:c.5245_5248delinsAACC XP_011520938.1:p.Asn1749=
XM_011522637.2:c.5242_5245delinsAACC XP_011520939.1:p.Asn1748=
XM_011522638.2:c.5407_5410delinsAACC XP_011520940.2:p.Asn1803=
XM_011522639.2:c.5116_5119delinsAACC XP_011520941.1:p.Asn1706=
XM_011522640.2:c.5113_5116delinsAACC XP_011520942.1:p.Asn1705=
XM_017023615.1:c.5188_5191delinsAACC XP_016879104.1:p.Asn1730=
XM_017023616.1:c.5059_5062delinsAACC XP_016879105.1:p.Asn1687=
XM_017023617.1:c.5155_5158delinsAACC XP_016879106.1:p.Asn1719=
XM_017023618.1:c.3901_3904delinsAACC XP_016879107.1:p.Asn1301=
XM_024450413.1:c.5077_5080delinsAACC XP_024306181.1:p.Asn1693=
NM_000548.5:c.5191_5194delinsAACC MANE Select NP_000539.2:p.Asn1731=
NM_001370404.1:c.5059_5062delinsAACC NP_001357333.1:p.Asn1687=
NM_001370405.1:c.5050_5053delinsAACC NP_001357334.1:p.Asn1684=
NM_001077183.3:c.4990_4993delinsAACC NP_001070651.1:p.Asn1664=
NM_001114382.3:c.5122_5125delinsAACC NP_001107854.1:p.Asn1708=
NM_001318827.2:c.4882_4885delinsAACC NP_001305756.1:p.Asn1628=
NM_001318829.2:c.4846_4849delinsAACC NP_001305758.1:p.Asn1616=
NM_001318831.2:c.4459_4462delinsAACC NP_001305760.1:p.Asn1487=
NM_001318832.2:c.5023_5026delinsAACC NP_001305761.1:p.Asn1675=
NM_001363528.2:c.4993_4996delinsAACC NP_001350457.1:p.Asn1665=
NM_021055.3:c.5062_5065delinsAACC NP_066399.2:p.Asn1688=