Canonical Allele Identifier: CA394292222
Gene: TSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2081658A>C , CM000678.2:g.2081658A>C GRCh38
NC_000016.9:g.2131659A>C , CM000678.1:g.2131659A>C GRCh37
NC_000016.8:g.2071660A>C NCBI36
NG_005895.1:g.37353A>C , LRG_487:g.37353A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2092A>C ENSP00000455997.2:n.*2092A>C
ENST00000642206.2:c.3590A>C ENSP00000495146.2:p.Asn1197Thr
ENST00000642365.2:c.3671A>C ENSP00000495459.2:p.Asn1224Thr
ENST00000644417.2:c.*4123A>C ENSP00000493912.2:n.*4123A>C
ENST00000646464.2:c.*4596A>C ENSP00000496610.2:n.*4596A>C
ENST00000219476.9:c.3674A>C MANE Select ENSP00000219476.3:p.Asn1225Thr
ENST00000350773.9:c.3674A>C ENSP00000344383.4:p.Asn1225Thr
ENST00000401874.7:c.3542A>C ENSP00000384468.2:p.Asn1181Thr
ENST00000568454.6:c.3575A>C ENSP00000454487.1:p.Asn1192Thr
ENST00000642365.1:c.2328A>C
ENST00000642561.1:c.3545A>C ENSP00000495099.1:p.Asn1182Thr
ENST00000642797.1:c.3545A>C ENSP00000493846.1:p.Asn1182Thr
ENST00000642936.1:c.3542A>C ENSP00000494514.1:p.Asn1181Thr
ENST00000643088.1:c.3542A>C ENSP00000494747.1:p.Asn1181Thr
ENST00000643426.1:n.1322A>C
ENST00000643533.1:n.184A>C
ENST00000643946.1:c.3674A>C ENSP00000495927.1:p.Asn1225Thr
ENST00000644043.1:c.3545A>C ENSP00000496262.1:p.Asn1182Thr
ENST00000644329.1:c.3542A>C ENSP00000496611.1:p.Asn1181Thr
ENST00000644335.1:c.3545A>C ENSP00000496317.1:p.Asn1182Thr
ENST00000644399.1:c.3664A>C
ENST00000644722.1:n.820A>C
ENST00000645024.1:n.1827A>C
ENST00000646388.1:c.3674A>C ENSP00000495921.1:p.Asn1225Thr
ENST00000646634.1:n.2558A>C
ENST00000646674.1:n.289A>C
ENST00000647042.1:n.966A>C
ENST00000647180.1:n.154A>C
ENST00000219476.7:c.3674A>C ENSP00000219476.3:p.Asn1225Thr
ENST00000350773.8:c.3674A>C ENSP00000344383.4:p.Asn1225Thr
ENST00000382538.10:c.3398A>C ENSP00000371978.6:p.Asn1133Thr
ENST00000401874.6:c.3542A>C ENSP00000384468.2:p.Asn1181Thr
ENST00000439117.6:c.*2841A>C ENSP00000406980.2:n.*2841A>C
ENST00000439673.6:c.3434A>C ENSP00000399232.2:p.Asn1145Thr
ENST00000497886.5:n.1501A>C
ENST00000568454.5:c.3575A>C ENSP00000454487.1:p.Asn1192Thr
NM_000548.3:c.3674A>C , LRG_487t1:c.3674A>C NP_000539.2:p.Asn1225Thr
NM_001077183.1:c.3542A>C NP_001070651.1:p.Asn1181Thr
NM_001114382.1:c.3674A>C NP_001107854.1:p.Asn1225Thr
XM_005255529.3:c.3545A>C XP_005255586.2:p.Asn1182Thr
XM_005255531.3:c.3545A>C XP_005255588.2:p.Asn1182Thr
XM_011522636.1:c.3674A>C XP_011520938.1:p.Asn1225Thr
XM_011522637.1:c.3671A>C XP_011520939.1:p.Asn1224Thr
XM_011522638.1:c.3563A>C XP_011520940.1:p.Asn1188Thr
XM_011522639.1:c.3545A>C XP_011520941.1:p.Asn1182Thr
XM_011522640.1:c.3542A>C XP_011520942.1:p.Asn1181Thr
XM_011522641.1:c.3434A>C XP_011520943.1:p.Asn1145Thr
NM_000548.4:c.3674A>C NP_000539.2:p.Asn1225Thr
NM_001077183.2:c.3542A>C NP_001070651.1:p.Asn1181Thr
NM_001114382.2:c.3674A>C NP_001107854.1:p.Asn1225Thr
NM_001318827.1:c.3434A>C NP_001305756.1:p.Asn1145Thr
NM_001318829.1:c.3398A>C NP_001305758.1:p.Asn1133Thr
NM_001318831.1:c.2942A>C NP_001305760.1:p.Asn981Thr
NM_001318832.1:c.3575A>C NP_001305761.1:p.Asn1192Thr
NM_001363528.1:c.3545A>C NP_001350457.1:p.Asn1182Thr
NM_021055.2:c.3545A>C NP_066399.2:p.Asn1182Thr
XM_005255531.4:c.3545A>C XP_005255588.2:p.Asn1182Thr
XM_011522636.2:c.3674A>C XP_011520938.1:p.Asn1225Thr
XM_011522637.2:c.3671A>C XP_011520939.1:p.Asn1224Thr
XM_011522638.2:c.3836A>C XP_011520940.2:p.Asn1279Thr
XM_011522639.2:c.3545A>C XP_011520941.1:p.Asn1182Thr
XM_011522640.2:c.3542A>C XP_011520942.1:p.Asn1181Thr
XM_017023615.1:c.3671A>C XP_016879104.1:p.Asn1224Thr
XM_017023616.1:c.3542A>C XP_016879105.1:p.Asn1181Thr
XM_017023617.1:c.3707A>C XP_016879106.1:p.Asn1236Thr
XM_017023618.1:c.2330A>C XP_016879107.1:p.Asn777Thr
XM_024450413.1:c.3542A>C XP_024306181.1:p.Asn1181Thr
NM_000548.5:c.3674A>C MANE Select NP_000539.2:p.Asn1225Thr
NM_001370404.1:c.3542A>C NP_001357333.1:p.Asn1181Thr
NM_001370405.1:c.3545A>C NP_001357334.1:p.Asn1182Thr
NM_001077183.3:c.3542A>C NP_001070651.1:p.Asn1181Thr
NM_001114382.3:c.3674A>C NP_001107854.1:p.Asn1225Thr
NM_001318827.2:c.3434A>C NP_001305756.1:p.Asn1145Thr
NM_001318829.2:c.3398A>C NP_001305758.1:p.Asn1133Thr
NM_001318831.2:c.2942A>C NP_001305760.1:p.Asn981Thr
NM_001318832.2:c.3575A>C NP_001305761.1:p.Asn1192Thr
NM_001363528.2:c.3545A>C NP_001350457.1:p.Asn1182Thr
NM_021055.3:c.3545A>C NP_066399.2:p.Asn1182Thr