Canonical Allele Identifier: CA394314515

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2138291G>T (hg19) ; chr16:g.2088290G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2088290G>T , CM000678.2:g.2088290G>T	GRCh38
NC_000016.9:g.2138291G>T , CM000678.1:g.2138291G>T	GRCh37
NC_000016.8:g.2078292G>T	NCBI36
NG_005895.1:g.43985G>T , LRG_487:g.43985G>T
NG_008617.1:g.54931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3573G>T	ENSP00000455997.2:n.*3573G>T
ENST00000642206.2:c.5071G>T	ENSP00000495146.2:p.Ala1691Ser
ENST00000642365.2:c.5221G>T	ENSP00000495459.2:p.Ala1741Ser
ENST00000644417.2:c.*5737G>T	ENSP00000493912.2:n.*5737G>T
ENST00000646464.2:c.*7973G>T	ENSP00000496610.2:n.*7973G>T
ENST00000219476.9:c.5224G>T MANE Select	ENSP00000219476.3:p.Ala1742Ser
ENST00000350773.9:c.5155G>T	ENSP00000344383.4:p.Ala1719Ser
ENST00000401874.7:c.5023G>T	ENSP00000384468.2:p.Ala1675Ser
ENST00000568454.6:c.5056G>T	ENSP00000454487.1:p.Ala1686Ser
ENST00000569110.2:c.1447G>T
ENST00000569930.2:n.3106G>T
ENST00000642365.1:c.3878G>T
ENST00000642561.1:c.5083G>T	ENSP00000495099.1:p.Ala1695Ser
ENST00000642791.1:n.821G>T
ENST00000642797.1:c.5026G>T	ENSP00000493846.1:p.Ala1676Ser
ENST00000642936.1:c.5092G>T	ENSP00000494514.1:p.Ala1698Ser
ENST00000643088.1:c.5017G>T	ENSP00000494747.1:p.Ala1673Ser
ENST00000643426.1:n.2872G>T
ENST00000643946.1:c.5149G>T	ENSP00000495927.1:p.Ala1717Ser
ENST00000644043.1:c.5095G>T	ENSP00000496262.1:p.Ala1699Ser
ENST00000644329.1:c.5110G>T	ENSP00000496611.1:p.Ala1704Ser
ENST00000644335.1:c.5020G>T	ENSP00000496317.1:p.Ala1674Ser
ENST00000644399.1:c.5145G>T
ENST00000645024.1:n.3308G>T
ENST00000646388.1:c.5218G>T	ENSP00000495921.1:p.Ala1740Ser
ENST00000646634.1:n.4039G>T
ENST00000646674.1:n.2476G>T
ENST00000647042.1:n.2447G>T
ENST00000647180.1:n.2337G>T
ENST00000219476.7:c.5224G>T	ENSP00000219476.3:p.Ala1742Ser
ENST00000350773.8:c.5155G>T	ENSP00000344383.4:p.Ala1719Ser
ENST00000382538.10:c.4879G>T	ENSP00000371978.6:p.Ala1627Ser
ENST00000401874.6:c.5023G>T	ENSP00000384468.2:p.Ala1675Ser
ENST00000439117.6:c.*4391G>T	ENSP00000406980.2:n.*4391G>T
ENST00000439673.6:c.4915G>T	ENSP00000399232.2:p.Ala1639Ser
ENST00000497886.5:n.2947G>T
ENST00000568454.5:c.5056G>T	ENSP00000454487.1:p.Ala1686Ser
ENST00000569110.1:c.1406G>T
ENST00000569930.1:n.2339G>T
NM_000548.3:c.5224G>T , LRG_487t1:c.5224G>T	NP_000539.2:p.Ala1742Ser
NM_001077183.1:c.5023G>T	NP_001070651.1:p.Ala1675Ser
NM_001114382.1:c.5155G>T	NP_001107854.1:p.Ala1719Ser
XM_005255529.3:c.5095G>T	XP_005255586.2:p.Ala1699Ser
XM_005255531.3:c.5026G>T	XP_005255588.2:p.Ala1676Ser
XM_011522636.1:c.5278G>T	XP_011520938.1:p.Ala1760Ser
XM_011522637.1:c.5275G>T	XP_011520939.1:p.Ala1759Ser
XM_011522638.1:c.5167G>T	XP_011520940.1:p.Ala1723Ser
XM_011522639.1:c.5149G>T	XP_011520941.1:p.Ala1717Ser
XM_011522640.1:c.5146G>T	XP_011520942.1:p.Ala1716Ser
XM_011522641.1:c.4915G>T	XP_011520943.1:p.Ala1639Ser
NM_000548.4:c.5224G>T	NP_000539.2:p.Ala1742Ser
NM_001077183.2:c.5023G>T	NP_001070651.1:p.Ala1675Ser
NM_001114382.2:c.5155G>T	NP_001107854.1:p.Ala1719Ser
NM_001318827.1:c.4915G>T	NP_001305756.1:p.Ala1639Ser
NM_001318829.1:c.4879G>T	NP_001305758.1:p.Ala1627Ser
NM_001318831.1:c.4492G>T	NP_001305760.1:p.Ala1498Ser
NM_001318832.1:c.5056G>T	NP_001305761.1:p.Ala1686Ser
NM_001363528.1:c.5026G>T	NP_001350457.1:p.Ala1676Ser
NM_021055.2:c.5095G>T	NP_066399.2:p.Ala1699Ser
XM_005255531.4:c.5026G>T	XP_005255588.2:p.Ala1676Ser
XM_011522636.2:c.5278G>T	XP_011520938.1:p.Ala1760Ser
XM_011522637.2:c.5275G>T	XP_011520939.1:p.Ala1759Ser
XM_011522638.2:c.5440G>T	XP_011520940.2:p.Ala1814Ser
XM_011522639.2:c.5149G>T	XP_011520941.1:p.Ala1717Ser
XM_011522640.2:c.5146G>T	XP_011520942.1:p.Ala1716Ser
XM_017023615.1:c.5221G>T	XP_016879104.1:p.Ala1741Ser
XM_017023616.1:c.5092G>T	XP_016879105.1:p.Ala1698Ser
XM_017023617.1:c.5188G>T	XP_016879106.1:p.Ala1730Ser
XM_017023618.1:c.3934G>T	XP_016879107.1:p.Ala1312Ser
XM_024450413.1:c.5110G>T	XP_024306181.1:p.Ala1704Ser
NM_000548.5:c.5224G>T MANE Select	NP_000539.2:p.Ala1742Ser
NM_001370404.1:c.5092G>T	NP_001357333.1:p.Ala1698Ser
NM_001370405.1:c.5083G>T	NP_001357334.1:p.Ala1695Ser
NM_001077183.3:c.5023G>T	NP_001070651.1:p.Ala1675Ser
NM_001114382.3:c.5155G>T	NP_001107854.1:p.Ala1719Ser
NM_001318827.2:c.4915G>T	NP_001305756.1:p.Ala1639Ser
NM_001318829.2:c.4879G>T	NP_001305758.1:p.Ala1627Ser
NM_001318831.2:c.4492G>T	NP_001305760.1:p.Ala1498Ser
NM_001318832.2:c.5056G>T	NP_001305761.1:p.Ala1686Ser
NM_001363528.2:c.5026G>T	NP_001350457.1:p.Ala1676Ser
NM_021055.3:c.5095G>T	NP_066399.2:p.Ala1699Ser