Canonical Allele Identifier: CA16615090

Gene: TSC2

Linked Data

• ClinVar Variation Id: 406076
• ClinVar RCV Id: RCV000465303 ; RCV000513743 ; RCV000574600
• dbSNP Id: rs45498892
• gnomAD v4: 16-2079356-C-T
• MyVariant Identifiers: chr16:g.2129357C>T (hg19) ; chr16:g.2079356C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2079356C>T , CM000678.2:g.2079356C>T	GRCh38
NC_000016.9:g.2129357C>T , CM000678.1:g.2129357C>T	GRCh37
NC_000016.8:g.2069358C>T	NCBI36
NG_005895.1:g.35051C>T , LRG_487:g.35051C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*1630C>T	ENSP00000455997.2:n.*1630C>T
ENST00000642206.2:c.3128C>T	ENSP00000495146.2:p.Thr1043Ile
ENST00000642365.2:c.3209C>T	ENSP00000495459.2:p.Thr1070Ile
ENST00000644417.2:c.*3661C>T	ENSP00000493912.2:n.*3661C>T
ENST00000646464.2:c.*4134C>T	ENSP00000496610.2:n.*4134C>T
ENST00000219476.9:c.3212C>T MANE Select	ENSP00000219476.3:p.Thr1071Ile
ENST00000350773.9:c.3212C>T	ENSP00000344383.4:p.Thr1071Ile
ENST00000401874.7:c.3080C>T	ENSP00000384468.2:p.Thr1027Ile
ENST00000471143.6:c.440C>T	ENSP00000458541.2:n.440C>T
ENST00000568454.6:c.3113C>T	ENSP00000454487.1:p.Thr1038Ile
ENST00000642365.1:c.1866C>T
ENST00000642561.1:c.3083C>T	ENSP00000495099.1:p.Thr1028Ile
ENST00000642797.1:c.3083C>T	ENSP00000493846.1:p.Thr1028Ile
ENST00000642936.1:c.3080C>T	ENSP00000494514.1:p.Thr1027Ile
ENST00000643088.1:c.3080C>T	ENSP00000494747.1:p.Thr1027Ile
ENST00000643946.1:c.3212C>T	ENSP00000495927.1:p.Thr1071Ile
ENST00000644043.1:c.3083C>T	ENSP00000496262.1:p.Thr1028Ile
ENST00000644329.1:c.3080C>T	ENSP00000496611.1:p.Thr1027Ile
ENST00000644335.1:c.3083C>T	ENSP00000496317.1:p.Thr1028Ile
ENST00000644399.1:c.3202C>T
ENST00000644722.1:n.358C>T
ENST00000645024.1:n.1365C>T
ENST00000646388.1:c.3212C>T	ENSP00000495921.1:p.Thr1071Ile
ENST00000646634.1:n.2096C>T
ENST00000647042.1:n.504C>T
ENST00000219476.7:c.3212C>T	ENSP00000219476.3:p.Thr1071Ile
ENST00000350773.8:c.3212C>T	ENSP00000344383.4:p.Thr1071Ile
ENST00000382538.10:c.2936C>T	ENSP00000371978.6:p.Thr979Ile
ENST00000401874.6:c.3080C>T	ENSP00000384468.2:p.Thr1027Ile
ENST00000439117.6:c.*2379C>T	ENSP00000406980.2:n.*2379C>T
ENST00000439673.6:c.2972C>T	ENSP00000399232.2:p.Thr991Ile
ENST00000471143.5:c.438C>T
ENST00000483020.5:c.452C>T	ENSP00000460310.1:n.452C>T
ENST00000497886.5:n.1039C>T
ENST00000561695.1:n.437C>T
ENST00000568366.5:n.569C>T
ENST00000568454.5:c.3113C>T	ENSP00000454487.1:p.Thr1038Ile
NM_000548.3:c.3212C>T , LRG_487t1:c.3212C>T	NP_000539.2:p.Thr1071Ile
NM_001077183.1:c.3080C>T	NP_001070651.1:p.Thr1027Ile
NM_001114382.1:c.3212C>T	NP_001107854.1:p.Thr1071Ile
XM_005255529.3:c.3083C>T	XP_005255586.2:p.Thr1028Ile
XM_005255531.3:c.3083C>T	XP_005255588.2:p.Thr1028Ile
XM_011522636.1:c.3212C>T	XP_011520938.1:p.Thr1071Ile
XM_011522637.1:c.3209C>T	XP_011520939.1:p.Thr1070Ile
XM_011522638.1:c.3101C>T	XP_011520940.1:p.Thr1034Ile
XM_011522639.1:c.3083C>T	XP_011520941.1:p.Thr1028Ile
XM_011522640.1:c.3080C>T	XP_011520942.1:p.Thr1027Ile
XM_011522641.1:c.2972C>T	XP_011520943.1:p.Thr991Ile
NM_000548.4:c.3212C>T	NP_000539.2:p.Thr1071Ile
NM_001077183.2:c.3080C>T	NP_001070651.1:p.Thr1027Ile
NM_001114382.2:c.3212C>T	NP_001107854.1:p.Thr1071Ile
NM_001318827.1:c.2972C>T	NP_001305756.1:p.Thr991Ile
NM_001318829.1:c.2936C>T	NP_001305758.1:p.Thr979Ile
NM_001318831.1:c.2480C>T	NP_001305760.1:p.Thr827Ile
NM_001318832.1:c.3113C>T	NP_001305761.1:p.Thr1038Ile
NM_001363528.1:c.3083C>T	NP_001350457.1:p.Thr1028Ile
NM_021055.2:c.3083C>T	NP_066399.2:p.Thr1028Ile
XM_005255531.4:c.3083C>T	XP_005255588.2:p.Thr1028Ile
XM_011522636.2:c.3212C>T	XP_011520938.1:p.Thr1071Ile
XM_011522637.2:c.3209C>T	XP_011520939.1:p.Thr1070Ile
XM_011522638.2:c.3374C>T	XP_011520940.2:p.Thr1125Ile
XM_011522639.2:c.3083C>T	XP_011520941.1:p.Thr1028Ile
XM_011522640.2:c.3080C>T	XP_011520942.1:p.Thr1027Ile
XM_017023615.1:c.3209C>T	XP_016879104.1:p.Thr1070Ile
XM_017023616.1:c.3080C>T	XP_016879105.1:p.Thr1027Ile
XM_017023617.1:c.3245C>T	XP_016879106.1:p.Thr1082Ile
XM_017023618.1:c.1868C>T	XP_016879107.1:p.Thr623Ile
XM_024450413.1:c.3080C>T	XP_024306181.1:p.Thr1027Ile
NM_000548.5:c.3212C>T MANE Select	NP_000539.2:p.Thr1071Ile
NM_001370404.1:c.3080C>T	NP_001357333.1:p.Thr1027Ile
NM_001370405.1:c.3083C>T	NP_001357334.1:p.Thr1028Ile
NM_001077183.3:c.3080C>T	NP_001070651.1:p.Thr1027Ile
NM_001114382.3:c.3212C>T	NP_001107854.1:p.Thr1071Ile
NM_001318827.2:c.2972C>T	NP_001305756.1:p.Thr991Ile
NM_001318829.2:c.2936C>T	NP_001305758.1:p.Thr979Ile
NM_001318831.2:c.2480C>T	NP_001305760.1:p.Thr827Ile
NM_001318832.2:c.3113C>T	NP_001305761.1:p.Thr1038Ile
NM_001363528.2:c.3083C>T	NP_001350457.1:p.Thr1028Ile
NM_021055.3:c.3083C>T	NP_066399.2:p.Thr1028Ile