Canonical Allele Identifier: CA2202019518

Gene: TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085298C= , CM000678.2:g.2085298C=	GRCh38
NC_000016.9:g.2135299C= , CM000678.1:g.2135299C=	GRCh37
NC_000016.8:g.2075300C=	NCBI36
NG_005895.1:g.40993C= , LRG_487:g.40993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2987C=	ENSP00000455997.2:n.*2987C=
ENST00000642206.2:c.4485C=	ENSP00000495146.2:p.Ala1495=
ENST00000642365.2:c.4635C=	ENSP00000495459.2:p.Ala1545=
ENST00000644417.2:c.*5018C=	ENSP00000493912.2:n.*5018C=
ENST00000646464.2:c.*7387C=	ENSP00000496610.2:n.*7387C=
ENST00000219476.9:c.4638C= MANE Select	ENSP00000219476.3:p.Ala1546=
ENST00000350773.9:c.4569C=	ENSP00000344383.4:p.Ala1523=
ENST00000401874.7:c.4437C=	ENSP00000384468.2:p.Ala1479=
ENST00000568454.6:c.4470C=	ENSP00000454487.1:p.Ala1490=
ENST00000569110.2:c.861C=
ENST00000569930.2:n.2520C=
ENST00000642365.1:c.3292C=
ENST00000642561.1:c.4509C=	ENSP00000495099.1:p.Ala1503=
ENST00000642728.1:n.820C=
ENST00000642791.1:n.235C=
ENST00000642797.1:c.4440C=	ENSP00000493846.1:p.Ala1480=
ENST00000642936.1:c.4506C=	ENSP00000494514.1:p.Ala1502=
ENST00000643088.1:c.4431C=	ENSP00000494747.1:p.Ala1477=
ENST00000643177.1:n.652C=
ENST00000643426.1:n.2286C=
ENST00000643946.1:c.4563C=	ENSP00000495927.1:p.Ala1521=
ENST00000644043.1:c.4509C=	ENSP00000496262.1:p.Ala1503=
ENST00000644278.1:n.120C=
ENST00000644329.1:c.4437C=	ENSP00000496611.1:p.Ala1479=
ENST00000644335.1:c.4434C=	ENSP00000496317.1:p.Ala1478=
ENST00000644399.1:c.4559C=
ENST00000645024.1:n.2722C=
ENST00000646388.1:c.4632C=	ENSP00000495921.1:p.Ala1544=
ENST00000646634.1:n.3453C=
ENST00000646674.1:n.1890C=
ENST00000647042.1:n.1861C=
ENST00000647180.1:n.1751C=
ENST00000219476.7:c.4638C=	ENSP00000219476.3:p.Ala1546=
ENST00000350773.8:c.4569C=	ENSP00000344383.4:p.Ala1523=
ENST00000382538.10:c.4293C=	ENSP00000371978.6:p.Ala1431=
ENST00000401874.6:c.4437C=	ENSP00000384468.2:p.Ala1479=
ENST00000439117.6:c.*3805C=	ENSP00000406980.2:n.*3805C=
ENST00000439673.6:c.4329C=	ENSP00000399232.2:p.Ala1443=
ENST00000497886.5:n.2396C=
ENST00000568454.5:c.4470C=	ENSP00000454487.1:p.Ala1490=
ENST00000569110.1:c.820C=
ENST00000569930.1:n.1753C=
NM_000548.3:c.4638C= , LRG_487t1:c.4638C=	NP_000539.2:p.Ala1546=
NM_001077183.1:c.4437C=	NP_001070651.1:p.Ala1479=
NM_001114382.1:c.4569C=	NP_001107854.1:p.Ala1523=
XM_005255529.3:c.4509C=	XP_005255586.2:p.Ala1503=
XM_005255531.3:c.4440C=	XP_005255588.2:p.Ala1480=
XM_011522636.1:c.4692C=	XP_011520938.1:p.Ala1564=
XM_011522637.1:c.4689C=	XP_011520939.1:p.Ala1563=
XM_011522638.1:c.4581C=	XP_011520940.1:p.Ala1527=
XM_011522639.1:c.4563C=	XP_011520941.1:p.Ala1521=
XM_011522640.1:c.4560C=	XP_011520942.1:p.Ala1520=
XM_011522641.1:c.4329C=	XP_011520943.1:p.Ala1443=
NM_000548.4:c.4638C=	NP_000539.2:p.Ala1546=
NM_001077183.2:c.4437C=	NP_001070651.1:p.Ala1479=
NM_001114382.2:c.4569C=	NP_001107854.1:p.Ala1523=
NM_001318827.1:c.4329C=	NP_001305756.1:p.Ala1443=
NM_001318829.1:c.4293C=	NP_001305758.1:p.Ala1431=
NM_001318831.1:c.3906C=	NP_001305760.1:p.Ala1302=
NM_001318832.1:c.4470C=	NP_001305761.1:p.Ala1490=
NM_001363528.1:c.4440C=	NP_001350457.1:p.Ala1480=
NM_021055.2:c.4509C=	NP_066399.2:p.Ala1503=
XM_005255531.4:c.4440C=	XP_005255588.2:p.Ala1480=
XM_011522636.2:c.4692C=	XP_011520938.1:p.Ala1564=
XM_011522637.2:c.4689C=	XP_011520939.1:p.Ala1563=
XM_011522638.2:c.4854C=	XP_011520940.2:p.Ala1618=
XM_011522639.2:c.4563C=	XP_011520941.1:p.Ala1521=
XM_011522640.2:c.4560C=	XP_011520942.1:p.Ala1520=
XM_017023615.1:c.4635C=	XP_016879104.1:p.Ala1545=
XM_017023616.1:c.4506C=	XP_016879105.1:p.Ala1502=
XM_017023617.1:c.4602C=	XP_016879106.1:p.Ala1534=
XM_017023618.1:c.3348C=	XP_016879107.1:p.Ala1116=
XM_024450413.1:c.4437C=	XP_024306181.1:p.Ala1479=
NM_000548.5:c.4638C= MANE Select	NP_000539.2:p.Ala1546=
NM_001370404.1:c.4506C=	NP_001357333.1:p.Ala1502=
NM_001370405.1:c.4509C=	NP_001357334.1:p.Ala1503=
NM_001077183.3:c.4437C=	NP_001070651.1:p.Ala1479=
NM_001114382.3:c.4569C=	NP_001107854.1:p.Ala1523=
NM_001318827.2:c.4329C=	NP_001305756.1:p.Ala1443=
NM_001318829.2:c.4293C=	NP_001305758.1:p.Ala1431=
NM_001318831.2:c.3906C=	NP_001305760.1:p.Ala1302=
NM_001318832.2:c.4470C=	NP_001305761.1:p.Ala1490=
NM_001363528.2:c.4440C=	NP_001350457.1:p.Ala1480=
NM_021055.3:c.4509C=	NP_066399.2:p.Ala1503=