Canonical Allele Identifier: CA2580091012

Gene: TSC2

Linked Data

• ClinVar Variation Id: 2004526
• ClinVar RCV Id: RCV002828301 ; RCV003738287

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2081632del , CM000678.2:g.2081632del	GRCh38
NC_000016.9:g.2131633del , CM000678.1:g.2131633del	GRCh37
NC_000016.8:g.2071634del	NCBI36
NG_005895.1:g.37327del , LRG_487:g.37327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2066del	ENSP00000455997.2:n.*2066del
ENST00000642206.2:c.3564del	ENSP00000495146.2:p.Ser1189AlafsTer?
ENST00000642365.2:c.3645del	ENSP00000495459.2:p.Ser1216AlafsTer?
ENST00000644417.2:c.*4097del	ENSP00000493912.2:n.*4097del
ENST00000646464.2:c.*4570del	ENSP00000496610.2:n.*4570del
ENST00000219476.9:c.3648del MANE Select	ENSP00000219476.3:p.Ser1217AlafsTer?
ENST00000350773.9:c.3648del	ENSP00000344383.4:p.Ser1217AlafsTer?
ENST00000401874.7:c.3516del	ENSP00000384468.2:p.Ser1173AlafsTer?
ENST00000568454.6:c.3549del	ENSP00000454487.1:p.Ser1184AlafsTer?
ENST00000642365.1:c.2302del
ENST00000642561.1:c.3519del	ENSP00000495099.1:p.Ser1174AlafsTer?
ENST00000642797.1:c.3519del	ENSP00000493846.1:p.Ser1174AlafsTer?
ENST00000642936.1:c.3516del	ENSP00000494514.1:p.Ser1173AlafsTer?
ENST00000643088.1:c.3516del	ENSP00000494747.1:p.Ser1173AlafsTer?
ENST00000643426.1:n.1296del
ENST00000643533.1:n.158del
ENST00000643946.1:c.3648del	ENSP00000495927.1:p.Ser1217AlafsTer?
ENST00000644043.1:c.3519del	ENSP00000496262.1:p.Ser1174AlafsTer?
ENST00000644329.1:c.3516del	ENSP00000496611.1:p.Ser1173AlafsTer?
ENST00000644335.1:c.3519del	ENSP00000496317.1:p.Ser1174AlafsTer?
ENST00000644399.1:c.3638del
ENST00000644722.1:n.794del
ENST00000645024.1:n.1801del
ENST00000646388.1:c.3648del	ENSP00000495921.1:p.Ser1217AlafsTer?
ENST00000646634.1:n.2532del
ENST00000646674.1:n.263del
ENST00000647042.1:n.940del
ENST00000647180.1:n.128del
ENST00000219476.7:c.3648del	ENSP00000219476.3:p.Ser1217AlafsTer?
ENST00000350773.8:c.3648del	ENSP00000344383.4:p.Ser1217AlafsTer?
ENST00000382538.10:c.3372del	ENSP00000371978.6:p.Ser1125AlafsTer?
ENST00000401874.6:c.3516del	ENSP00000384468.2:p.Ser1173AlafsTer?
ENST00000439117.6:c.*2815del	ENSP00000406980.2:n.*2815del
ENST00000439673.6:c.3408del	ENSP00000399232.2:p.Ser1137AlafsTer?
ENST00000497886.5:n.1475del
ENST00000568454.5:c.3549del	ENSP00000454487.1:p.Ser1184AlafsTer?
NM_000548.3:c.3648del , LRG_487t1:c.3648del	NP_000539.2:p.Ser1217AlafsTer?
NM_001077183.1:c.3516del	NP_001070651.1:p.Ser1173AlafsTer?
NM_001114382.1:c.3648del	NP_001107854.1:p.Ser1217AlafsTer?
XM_005255529.3:c.3519del	XP_005255586.2:p.Ser1174AlafsTer?
XM_005255531.3:c.3519del	XP_005255588.2:p.Ser1174AlafsTer?
XM_011522636.1:c.3648del	XP_011520938.1:p.Ser1217AlafsTer?
XM_011522637.1:c.3645del	XP_011520939.1:p.Ser1216AlafsTer?
XM_011522638.1:c.3537del	XP_011520940.1:p.Ser1180AlafsTer?
XM_011522639.1:c.3519del	XP_011520941.1:p.Ser1174AlafsTer?
XM_011522640.1:c.3516del	XP_011520942.1:p.Ser1173AlafsTer?
XM_011522641.1:c.3408del	XP_011520943.1:p.Ser1137AlafsTer?
NM_000548.4:c.3648del	NP_000539.2:p.Ser1217AlafsTer?
NM_001077183.2:c.3516del	NP_001070651.1:p.Ser1173AlafsTer?
NM_001114382.2:c.3648del	NP_001107854.1:p.Ser1217AlafsTer?
NM_001318827.1:c.3408del	NP_001305756.1:p.Ser1137AlafsTer?
NM_001318829.1:c.3372del	NP_001305758.1:p.Ser1125AlafsTer?
NM_001318831.1:c.2916del	NP_001305760.1:p.Ser973AlafsTer?
NM_001318832.1:c.3549del	NP_001305761.1:p.Ser1184AlafsTer?
NM_001363528.1:c.3519del	NP_001350457.1:p.Ser1174AlafsTer?
NM_021055.2:c.3519del	NP_066399.2:p.Ser1174AlafsTer?
XM_005255531.4:c.3519del	XP_005255588.2:p.Ser1174AlafsTer?
XM_011522636.2:c.3648del	XP_011520938.1:p.Ser1217AlafsTer?
XM_011522637.2:c.3645del	XP_011520939.1:p.Ser1216AlafsTer?
XM_011522638.2:c.3810del	XP_011520940.2:p.Ser1271AlafsTer?
XM_011522639.2:c.3519del	XP_011520941.1:p.Ser1174AlafsTer?
XM_011522640.2:c.3516del	XP_011520942.1:p.Ser1173AlafsTer?
XM_017023615.1:c.3645del	XP_016879104.1:p.Ser1216AlafsTer?
XM_017023616.1:c.3516del	XP_016879105.1:p.Ser1173AlafsTer?
XM_017023617.1:c.3681del	XP_016879106.1:p.Ser1228AlafsTer?
XM_017023618.1:c.2304del	XP_016879107.1:p.Ser769AlafsTer?
XM_024450413.1:c.3516del	XP_024306181.1:p.Ser1173AlafsTer?
NM_000548.5:c.3648del MANE Select	NP_000539.2:p.Ser1217AlafsTer?
NM_001370404.1:c.3516del	NP_001357333.1:p.Ser1173AlafsTer?
NM_001370405.1:c.3519del	NP_001357334.1:p.Ser1174AlafsTer?
NM_001077183.3:c.3516del	NP_001070651.1:p.Ser1173AlafsTer?
NM_001114382.3:c.3648del	NP_001107854.1:p.Ser1217AlafsTer?
NM_001318827.2:c.3408del	NP_001305756.1:p.Ser1137AlafsTer?
NM_001318829.2:c.3372del	NP_001305758.1:p.Ser1125AlafsTer?
NM_001318831.2:c.2916del	NP_001305760.1:p.Ser973AlafsTer?
NM_001318832.2:c.3549del	NP_001305761.1:p.Ser1184AlafsTer?
NM_001363528.2:c.3519del	NP_001350457.1:p.Ser1174AlafsTer?
NM_021055.3:c.3519del	NP_066399.2:p.Ser1174AlafsTer?