Canonical Allele Identifier: CA394291418
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 648981
ClinVar RCV Id: RCV000803826
dbSNP Id: rs924403519

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2081599C>G , CM000678.2:g.2081599C>G GRCh38
NC_000016.9:g.2131600C>G , CM000678.1:g.2131600C>G GRCh37
NC_000016.8:g.2071601C>G NCBI36
NG_005895.1:g.37294C>G , LRG_487:g.37294C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2033C>G ENSP00000455997.2:n.*2033C>G
ENST00000642206.2:c.3531C>G ENSP00000495146.2:p.Asn1177Lys
ENST00000642365.2:c.3612C>G ENSP00000495459.2:p.Asn1204Lys
ENST00000644417.2:c.*4064C>G ENSP00000493912.2:n.*4064C>G
ENST00000646464.2:c.*4537C>G ENSP00000496610.2:n.*4537C>G
ENST00000219476.9:c.3615C>G MANE Select ENSP00000219476.3:p.Asn1205Lys
ENST00000350773.9:c.3615C>G ENSP00000344383.4:p.Asn1205Lys
ENST00000401874.7:c.3483C>G ENSP00000384468.2:p.Asn1161Lys
ENST00000568454.6:c.3516C>G ENSP00000454487.1:p.Asn1172Lys
ENST00000642365.1:c.2269C>G
ENST00000642561.1:c.3486C>G ENSP00000495099.1:p.Asn1162Lys
ENST00000642797.1:c.3486C>G ENSP00000493846.1:p.Asn1162Lys
ENST00000642936.1:c.3483C>G ENSP00000494514.1:p.Asn1161Lys
ENST00000643088.1:c.3483C>G ENSP00000494747.1:p.Asn1161Lys
ENST00000643426.1:n.1263C>G
ENST00000643533.1:n.125C>G
ENST00000643946.1:c.3615C>G ENSP00000495927.1:p.Asn1205Lys
ENST00000644043.1:c.3486C>G ENSP00000496262.1:p.Asn1162Lys
ENST00000644329.1:c.3483C>G ENSP00000496611.1:p.Asn1161Lys
ENST00000644335.1:c.3486C>G ENSP00000496317.1:p.Asn1162Lys
ENST00000644399.1:c.3605C>G
ENST00000644722.1:n.761C>G
ENST00000645024.1:n.1768C>G
ENST00000646388.1:c.3615C>G ENSP00000495921.1:p.Asn1205Lys
ENST00000646634.1:n.2499C>G
ENST00000646674.1:n.230C>G
ENST00000647042.1:n.907C>G
ENST00000647180.1:n.95C>G
ENST00000219476.7:c.3615C>G ENSP00000219476.3:p.Asn1205Lys
ENST00000350773.8:c.3615C>G ENSP00000344383.4:p.Asn1205Lys
ENST00000382538.10:c.3339C>G ENSP00000371978.6:p.Asn1113Lys
ENST00000401874.6:c.3483C>G ENSP00000384468.2:p.Asn1161Lys
ENST00000439117.6:c.*2782C>G ENSP00000406980.2:n.*2782C>G
ENST00000439673.6:c.3375C>G ENSP00000399232.2:p.Asn1125Lys
ENST00000497886.5:n.1442C>G
ENST00000568454.5:c.3516C>G ENSP00000454487.1:p.Asn1172Lys
NM_000548.3:c.3615C>G , LRG_487t1:c.3615C>G NP_000539.2:p.Asn1205Lys
NM_001077183.1:c.3483C>G NP_001070651.1:p.Asn1161Lys
NM_001114382.1:c.3615C>G NP_001107854.1:p.Asn1205Lys
XM_005255529.3:c.3486C>G XP_005255586.2:p.Asn1162Lys
XM_005255531.3:c.3486C>G XP_005255588.2:p.Asn1162Lys
XM_011522636.1:c.3615C>G XP_011520938.1:p.Asn1205Lys
XM_011522637.1:c.3612C>G XP_011520939.1:p.Asn1204Lys
XM_011522638.1:c.3504C>G XP_011520940.1:p.Asn1168Lys
XM_011522639.1:c.3486C>G XP_011520941.1:p.Asn1162Lys
XM_011522640.1:c.3483C>G XP_011520942.1:p.Asn1161Lys
XM_011522641.1:c.3375C>G XP_011520943.1:p.Asn1125Lys
NM_000548.4:c.3615C>G NP_000539.2:p.Asn1205Lys
NM_001077183.2:c.3483C>G NP_001070651.1:p.Asn1161Lys
NM_001114382.2:c.3615C>G NP_001107854.1:p.Asn1205Lys
NM_001318827.1:c.3375C>G NP_001305756.1:p.Asn1125Lys
NM_001318829.1:c.3339C>G NP_001305758.1:p.Asn1113Lys
NM_001318831.1:c.2883C>G NP_001305760.1:p.Asn961Lys
NM_001318832.1:c.3516C>G NP_001305761.1:p.Asn1172Lys
NM_001363528.1:c.3486C>G NP_001350457.1:p.Asn1162Lys
NM_021055.2:c.3486C>G NP_066399.2:p.Asn1162Lys
XM_005255531.4:c.3486C>G XP_005255588.2:p.Asn1162Lys
XM_011522636.2:c.3615C>G XP_011520938.1:p.Asn1205Lys
XM_011522637.2:c.3612C>G XP_011520939.1:p.Asn1204Lys
XM_011522638.2:c.3777C>G XP_011520940.2:p.Asn1259Lys
XM_011522639.2:c.3486C>G XP_011520941.1:p.Asn1162Lys
XM_011522640.2:c.3483C>G XP_011520942.1:p.Asn1161Lys
XM_017023615.1:c.3612C>G XP_016879104.1:p.Asn1204Lys
XM_017023616.1:c.3483C>G XP_016879105.1:p.Asn1161Lys
XM_017023617.1:c.3648C>G XP_016879106.1:p.Asn1216Lys
XM_017023618.1:c.2271C>G XP_016879107.1:p.Asn757Lys
XM_024450413.1:c.3483C>G XP_024306181.1:p.Asn1161Lys
NM_000548.5:c.3615C>G MANE Select NP_000539.2:p.Asn1205Lys
NM_001370404.1:c.3483C>G NP_001357333.1:p.Asn1161Lys
NM_001370405.1:c.3486C>G NP_001357334.1:p.Asn1162Lys
NM_001077183.3:c.3483C>G NP_001070651.1:p.Asn1161Lys
NM_001114382.3:c.3615C>G NP_001107854.1:p.Asn1205Lys
NM_001318827.2:c.3375C>G NP_001305756.1:p.Asn1125Lys
NM_001318829.2:c.3339C>G NP_001305758.1:p.Asn1113Lys
NM_001318831.2:c.2883C>G NP_001305760.1:p.Asn961Lys
NM_001318832.2:c.3516C>G NP_001305761.1:p.Asn1172Lys
NM_001363528.2:c.3486C>G NP_001350457.1:p.Asn1162Lys
NM_021055.3:c.3486C>G NP_066399.2:p.Asn1162Lys