Canonical Allele Identifier: CA2202028571
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2079288C= , CM000678.2:g.2079288C= GRCh38
NC_000016.9:g.2129289C= , CM000678.1:g.2129289C= GRCh37
NC_000016.8:g.2069290C= NCBI36
NG_005895.1:g.34983C= , LRG_487:g.34983C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*1562C= ENSP00000455997.2:n.*1562C=
ENST00000642206.2:c.3060C= ENSP00000495146.2:p.Gly1020=
ENST00000642365.2:c.3141C= ENSP00000495459.2:p.Gly1047=
ENST00000644417.2:c.*3593C= ENSP00000493912.2:n.*3593C=
ENST00000646464.2:c.*4066C= ENSP00000496610.2:n.*4066C=
ENST00000219476.9:c.3144C= MANE Select ENSP00000219476.3:p.Gly1048=
ENST00000350773.9:c.3144C= ENSP00000344383.4:p.Gly1048=
ENST00000401874.7:c.3012C= ENSP00000384468.2:p.Gly1004=
ENST00000471143.6:c.372C= ENSP00000458541.2:n.372C=
ENST00000568366.6:n.501C=
ENST00000568454.6:c.3045C= ENSP00000454487.1:p.Gly1015=
ENST00000642365.1:c.1798C=
ENST00000642561.1:c.3015C= ENSP00000495099.1:p.Gly1005=
ENST00000642797.1:c.3015C= ENSP00000493846.1:p.Gly1005=
ENST00000642936.1:c.3012C= ENSP00000494514.1:p.Gly1004=
ENST00000643088.1:c.3012C= ENSP00000494747.1:p.Gly1004=
ENST00000643946.1:c.3144C= ENSP00000495927.1:p.Gly1048=
ENST00000644043.1:c.3015C= ENSP00000496262.1:p.Gly1005=
ENST00000644329.1:c.3012C= ENSP00000496611.1:p.Gly1004=
ENST00000644335.1:c.3015C= ENSP00000496317.1:p.Gly1005=
ENST00000644399.1:c.3134C=
ENST00000644722.1:n.290C=
ENST00000645024.1:n.1297C=
ENST00000646388.1:c.3144C= ENSP00000495921.1:p.Gly1048=
ENST00000646634.1:n.2028C=
ENST00000647042.1:n.436C=
ENST00000219476.7:c.3144C= ENSP00000219476.3:p.Gly1048=
ENST00000350773.8:c.3144C= ENSP00000344383.4:p.Gly1048=
ENST00000382538.10:c.2868C= ENSP00000371978.6:p.Gly956=
ENST00000401874.6:c.3012C= ENSP00000384468.2:p.Gly1004=
ENST00000439117.6:c.*2311C= ENSP00000406980.2:n.*2311C=
ENST00000439673.6:c.2904C= ENSP00000399232.2:p.Gly968=
ENST00000471143.5:c.370C=
ENST00000483020.5:c.384C= ENSP00000460310.1:n.384C=
ENST00000497886.5:n.971C=
ENST00000561695.1:n.369C=
ENST00000568366.5:n.501C=
ENST00000568454.5:c.3045C= ENSP00000454487.1:p.Gly1015=
NM_000548.3:c.3144C= , LRG_487t1:c.3144C= NP_000539.2:p.Gly1048=
NM_001077183.1:c.3012C= NP_001070651.1:p.Gly1004=
NM_001114382.1:c.3144C= NP_001107854.1:p.Gly1048=
XM_005255529.3:c.3015C= XP_005255586.2:p.Gly1005=
XM_005255531.3:c.3015C= XP_005255588.2:p.Gly1005=
XM_011522636.1:c.3144C= XP_011520938.1:p.Gly1048=
XM_011522637.1:c.3141C= XP_011520939.1:p.Gly1047=
XM_011522638.1:c.3033C= XP_011520940.1:p.Gly1011=
XM_011522639.1:c.3015C= XP_011520941.1:p.Gly1005=
XM_011522640.1:c.3012C= XP_011520942.1:p.Gly1004=
XM_011522641.1:c.2904C= XP_011520943.1:p.Gly968=
NM_000548.4:c.3144C= NP_000539.2:p.Gly1048=
NM_001077183.2:c.3012C= NP_001070651.1:p.Gly1004=
NM_001114382.2:c.3144C= NP_001107854.1:p.Gly1048=
NM_001318827.1:c.2904C= NP_001305756.1:p.Gly968=
NM_001318829.1:c.2868C= NP_001305758.1:p.Gly956=
NM_001318831.1:c.2412C= NP_001305760.1:p.Gly804=
NM_001318832.1:c.3045C= NP_001305761.1:p.Gly1015=
NM_001363528.1:c.3015C= NP_001350457.1:p.Gly1005=
NM_021055.2:c.3015C= NP_066399.2:p.Gly1005=
XM_005255531.4:c.3015C= XP_005255588.2:p.Gly1005=
XM_011522636.2:c.3144C= XP_011520938.1:p.Gly1048=
XM_011522637.2:c.3141C= XP_011520939.1:p.Gly1047=
XM_011522638.2:c.3306C= XP_011520940.2:p.Gly1102=
XM_011522639.2:c.3015C= XP_011520941.1:p.Gly1005=
XM_011522640.2:c.3012C= XP_011520942.1:p.Gly1004=
XM_017023615.1:c.3141C= XP_016879104.1:p.Gly1047=
XM_017023616.1:c.3012C= XP_016879105.1:p.Gly1004=
XM_017023617.1:c.3177C= XP_016879106.1:p.Gly1059=
XM_017023618.1:c.1800C= XP_016879107.1:p.Gly600=
XM_024450413.1:c.3012C= XP_024306181.1:p.Gly1004=
NM_000548.5:c.3144C= MANE Select NP_000539.2:p.Gly1048=
NM_001370404.1:c.3012C= NP_001357333.1:p.Gly1004=
NM_001370405.1:c.3015C= NP_001357334.1:p.Gly1005=
NM_001077183.3:c.3012C= NP_001070651.1:p.Gly1004=
NM_001114382.3:c.3144C= NP_001107854.1:p.Gly1048=
NM_001318827.2:c.2904C= NP_001305756.1:p.Gly968=
NM_001318829.2:c.2868C= NP_001305758.1:p.Gly956=
NM_001318831.2:c.2412C= NP_001305760.1:p.Gly804=
NM_001318832.2:c.3045C= NP_001305761.1:p.Gly1015=
NM_001363528.2:c.3015C= NP_001350457.1:p.Gly1005=
NM_021055.3:c.3015C= NP_066399.2:p.Gly1005=