Canonical Allele Identifier: CA2739265845

Gene: TSC2

Linked Data

• ClinVar Variation Id: 2864367
• ClinVar RCV Id: RCV003626288

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084934_2084942del , CM000678.2:g.2084934_2084942del	GRCh38
NC_000016.9:g.2134935_2134943del , CM000678.1:g.2134935_2134943del	GRCh37
NC_000016.8:g.2074936_2074944del	NCBI36
NG_005895.1:g.40629_40637del , LRG_487:g.40629_40637del

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*2843-17_*2843-9del	ENSP00000455997.2:n.*2843-17_*2843-9del
ENST00000642206.2:c.4341-17_4341-9del	ENSP00000495146.2:n.4341-17_4341-9del
ENST00000642365.2:c.4491-17_4491-9del	ENSP00000495459.2:n.4491-17_4491-9del
ENST00000644417.2:c.*4874-17_*4874-9del	ENSP00000493912.2:n.*4874-17_*4874-9del
ENST00000646464.2:c.*7243-17_*7243-9del	ENSP00000496610.2:n.*7243-17_*7243-9del
ENST00000219476.9:c.4494-17_4494-9del MANE Select	ENSP00000219476.3:n.4494-17_4494-9del
ENST00000350773.9:c.4425-17_4425-9del	ENSP00000344383.4:n.4425-17_4425-9del
ENST00000401874.7:c.4293-17_4293-9del	ENSP00000384468.2:n.4293-17_4293-9del
ENST00000568454.6:c.4326-17_4326-9del	ENSP00000454487.1:n.4326-17_4326-9del
ENST00000569110.2:c.717-17_717-9del
ENST00000569930.2:n.2376-17_2376-9del
ENST00000642365.1:c.3148-17_3148-9del
ENST00000642561.1:c.4365-17_4365-9del	ENSP00000495099.1:n.4365-17_4365-9del
ENST00000642728.1:n.676-17_676-9del
ENST00000642797.1:c.4296-17_4296-9del	ENSP00000493846.1:n.4296-17_4296-9del
ENST00000642936.1:c.4362-17_4362-9del	ENSP00000494514.1:n.4362-17_4362-9del
ENST00000643088.1:c.4293-17_4293-9del	ENSP00000494747.1:n.4293-17_4293-9del
ENST00000643177.1:n.508-17_508-9del
ENST00000643426.1:n.2142-17_2142-9del
ENST00000643946.1:c.4425-17_4425-9del	ENSP00000495927.1:n.4425-17_4425-9del
ENST00000644043.1:c.4365-17_4365-9del	ENSP00000496262.1:n.4365-17_4365-9del
ENST00000644329.1:c.4293-17_4293-9del	ENSP00000496611.1:n.4293-17_4293-9del
ENST00000644335.1:c.4296-17_4296-9del	ENSP00000496317.1:n.4296-17_4296-9del
ENST00000644399.1:c.4415-17_4415-9del
ENST00000645024.1:n.2578-17_2578-9del
ENST00000646388.1:c.4494-17_4494-9del	ENSP00000495921.1:n.4494-17_4494-9del
ENST00000646634.1:n.3309-17_3309-9del
ENST00000646674.1:n.1746-17_1746-9del
ENST00000647042.1:n.1717-17_1717-9del
ENST00000647180.1:n.1607-17_1607-9del
ENST00000219476.7:c.4494-17_4494-9del	ENSP00000219476.3:n.4494-17_4494-9del
ENST00000350773.8:c.4425-17_4425-9del	ENSP00000344383.4:n.4425-17_4425-9del
ENST00000382538.10:c.4149-17_4149-9del	ENSP00000371978.6:n.4149-17_4149-9del
ENST00000401874.6:c.4293-17_4293-9del	ENSP00000384468.2:n.4293-17_4293-9del
ENST00000439117.6:c.*3661-17_*3661-9del	ENSP00000406980.2:n.*3661-17_*3661-9del
ENST00000439673.6:c.4185-17_4185-9del	ENSP00000399232.2:n.4185-17_4185-9del
ENST00000497886.5:n.2252-17_2252-9del
ENST00000568454.5:c.4326-17_4326-9del	ENSP00000454487.1:n.4326-17_4326-9del
ENST00000569110.1:c.676-17_676-9del
ENST00000569930.1:n.1609-17_1609-9del
NM_000548.3:c.4494-17_4494-9del , LRG_487t1:c.4494-17_4494-9del	NP_000539.2:n.4494-17_4494-9del
NM_001077183.1:c.4293-17_4293-9del	NP_001070651.1:n.4293-17_4293-9del
NM_001114382.1:c.4425-17_4425-9del	NP_001107854.1:n.4425-17_4425-9del
XM_005255529.3:c.4365-17_4365-9del	XP_005255586.2:n.4365-17_4365-9del
XM_005255531.3:c.4296-17_4296-9del	XP_005255588.2:n.4296-17_4296-9del
XM_011522636.1:c.4548-17_4548-9del	XP_011520938.1:n.4548-17_4548-9del
XM_011522637.1:c.4545-17_4545-9del	XP_011520939.1:n.4545-17_4545-9del
XM_011522638.1:c.4437-17_4437-9del	XP_011520940.1:n.4437-17_4437-9del
XM_011522639.1:c.4419-17_4419-9del	XP_011520941.1:n.4419-17_4419-9del
XM_011522640.1:c.4416-17_4416-9del	XP_011520942.1:n.4416-17_4416-9del
XM_011522641.1:c.4185-17_4185-9del	XP_011520943.1:n.4185-17_4185-9del
NM_000548.4:c.4494-17_4494-9del	NP_000539.2:n.4494-17_4494-9del
NM_001077183.2:c.4293-17_4293-9del	NP_001070651.1:n.4293-17_4293-9del
NM_001114382.2:c.4425-17_4425-9del	NP_001107854.1:n.4425-17_4425-9del
NM_001318827.1:c.4185-17_4185-9del	NP_001305756.1:n.4185-17_4185-9del
NM_001318829.1:c.4149-17_4149-9del	NP_001305758.1:n.4149-17_4149-9del
NM_001318831.1:c.3762-17_3762-9del	NP_001305760.1:n.3762-17_3762-9del
NM_001318832.1:c.4326-17_4326-9del	NP_001305761.1:n.4326-17_4326-9del
NM_001363528.1:c.4296-17_4296-9del	NP_001350457.1:n.4296-17_4296-9del
NM_021055.2:c.4365-17_4365-9del	NP_066399.2:n.4365-17_4365-9del
XM_005255531.4:c.4296-17_4296-9del	XP_005255588.2:n.4296-17_4296-9del
XM_011522636.2:c.4548-17_4548-9del	XP_011520938.1:n.4548-17_4548-9del
XM_011522637.2:c.4545-17_4545-9del	XP_011520939.1:n.4545-17_4545-9del
XM_011522638.2:c.4710-17_4710-9del	XP_011520940.2:n.4710-17_4710-9del
XM_011522639.2:c.4419-17_4419-9del	XP_011520941.1:n.4419-17_4419-9del
XM_011522640.2:c.4416-17_4416-9del	XP_011520942.1:n.4416-17_4416-9del
XM_017023615.1:c.4491-17_4491-9del	XP_016879104.1:n.4491-17_4491-9del
XM_017023616.1:c.4362-17_4362-9del	XP_016879105.1:n.4362-17_4362-9del
XM_017023617.1:c.4458-17_4458-9del	XP_016879106.1:n.4458-17_4458-9del
XM_017023618.1:c.3204-17_3204-9del	XP_016879107.1:n.3204-17_3204-9del
XM_024450413.1:c.4293-17_4293-9del	XP_024306181.1:n.4293-17_4293-9del
NM_000548.5:c.4494-17_4494-9del MANE Select	NP_000539.2:n.4494-17_4494-9del
NM_001370404.1:c.4362-17_4362-9del	NP_001357333.1:n.4362-17_4362-9del
NM_001370405.1:c.4365-17_4365-9del	NP_001357334.1:n.4365-17_4365-9del
NM_001077183.3:c.4293-17_4293-9del	NP_001070651.1:n.4293-17_4293-9del
NM_001114382.3:c.4425-17_4425-9del	NP_001107854.1:n.4425-17_4425-9del
NM_001318827.2:c.4185-17_4185-9del	NP_001305756.1:n.4185-17_4185-9del
NM_001318829.2:c.4149-17_4149-9del	NP_001305758.1:n.4149-17_4149-9del
NM_001318831.2:c.3762-17_3762-9del	NP_001305760.1:n.3762-17_3762-9del
NM_001318832.2:c.4326-17_4326-9del	NP_001305761.1:n.4326-17_4326-9del
NM_001363528.2:c.4296-17_4296-9del	NP_001350457.1:n.4296-17_4296-9del
NM_021055.3:c.4365-17_4365-9del	NP_066399.2:n.4365-17_4365-9del