Canonical Allele Identifier: CA394301334

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2134545C>G (hg19) ; chr16:g.2084544C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084544C>G , CM000678.2:g.2084544C>G	GRCh38
NC_000016.9:g.2134545C>G , CM000678.1:g.2134545C>G	GRCh37
NC_000016.8:g.2074546C>G	NCBI36
NG_005895.1:g.40239C>G , LRG_487:g.40239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2671C>G	ENSP00000455997.2:n.*2671C>G
ENST00000642206.2:c.4169C>G	ENSP00000495146.2:p.Pro1390Arg
ENST00000642365.2:c.4319C>G	ENSP00000495459.2:p.Pro1440Arg
ENST00000644417.2:c.*4702C>G	ENSP00000493912.2:n.*4702C>G
ENST00000646464.2:c.*7071C>G	ENSP00000496610.2:n.*7071C>G
ENST00000219476.9:c.4322C>G MANE Select	ENSP00000219476.3:p.Pro1441Arg
ENST00000350773.9:c.4253C>G	ENSP00000344383.4:p.Pro1418Arg
ENST00000401874.7:c.4121C>G	ENSP00000384468.2:p.Pro1374Arg
ENST00000568454.6:c.4154C>G	ENSP00000454487.1:p.Pro1385Arg
ENST00000569110.2:c.558C>G
ENST00000569930.2:n.2204C>G
ENST00000642365.1:c.2976C>G
ENST00000642561.1:c.4193C>G	ENSP00000495099.1:p.Pro1398Arg
ENST00000642728.1:n.504C>G
ENST00000642797.1:c.4124C>G	ENSP00000493846.1:p.Pro1375Arg
ENST00000642936.1:c.4190C>G	ENSP00000494514.1:p.Pro1397Arg
ENST00000643088.1:c.4121C>G	ENSP00000494747.1:p.Pro1374Arg
ENST00000643177.1:n.336C>G
ENST00000643426.1:n.1970C>G
ENST00000643946.1:c.4253C>G	ENSP00000495927.1:p.Pro1418Arg
ENST00000644043.1:c.4193C>G	ENSP00000496262.1:p.Pro1398Arg
ENST00000644329.1:c.4121C>G	ENSP00000496611.1:p.Pro1374Arg
ENST00000644335.1:c.4124C>G	ENSP00000496317.1:p.Pro1375Arg
ENST00000644399.1:c.4243C>G
ENST00000645024.1:n.2406C>G
ENST00000646388.1:c.4322C>G	ENSP00000495921.1:p.Pro1441Arg
ENST00000646634.1:n.3137C>G
ENST00000646674.1:n.1574C>G
ENST00000647042.1:n.1545C>G
ENST00000647180.1:n.1435C>G
ENST00000219476.7:c.4322C>G	ENSP00000219476.3:p.Pro1441Arg
ENST00000350773.8:c.4253C>G	ENSP00000344383.4:p.Pro1418Arg
ENST00000382538.10:c.3977C>G	ENSP00000371978.6:p.Pro1326Arg
ENST00000401874.6:c.4121C>G	ENSP00000384468.2:p.Pro1374Arg
ENST00000439117.6:c.*3489C>G	ENSP00000406980.2:n.*3489C>G
ENST00000439673.6:c.4013C>G	ENSP00000399232.2:p.Pro1338Arg
ENST00000497886.5:n.2080C>G
ENST00000568454.5:c.4154C>G	ENSP00000454487.1:p.Pro1385Arg
ENST00000569110.1:c.504C>G
ENST00000569930.1:n.1437C>G
NM_000548.3:c.4322C>G , LRG_487t1:c.4322C>G	NP_000539.2:p.Pro1441Arg
NM_001077183.1:c.4121C>G	NP_001070651.1:p.Pro1374Arg
NM_001114382.1:c.4253C>G	NP_001107854.1:p.Pro1418Arg
XM_005255529.3:c.4193C>G	XP_005255586.2:p.Pro1398Arg
XM_005255531.3:c.4124C>G	XP_005255588.2:p.Pro1375Arg
XM_011522636.1:c.4376C>G	XP_011520938.1:p.Pro1459Arg
XM_011522637.1:c.4373C>G	XP_011520939.1:p.Pro1458Arg
XM_011522638.1:c.4265C>G	XP_011520940.1:p.Pro1422Arg
XM_011522639.1:c.4247C>G	XP_011520941.1:p.Pro1416Arg
XM_011522640.1:c.4244C>G	XP_011520942.1:p.Pro1415Arg
XM_011522641.1:c.4013C>G	XP_011520943.1:p.Pro1338Arg
NM_000548.4:c.4322C>G	NP_000539.2:p.Pro1441Arg
NM_001077183.2:c.4121C>G	NP_001070651.1:p.Pro1374Arg
NM_001114382.2:c.4253C>G	NP_001107854.1:p.Pro1418Arg
NM_001318827.1:c.4013C>G	NP_001305756.1:p.Pro1338Arg
NM_001318829.1:c.3977C>G	NP_001305758.1:p.Pro1326Arg
NM_001318831.1:c.3590C>G	NP_001305760.1:p.Pro1197Arg
NM_001318832.1:c.4154C>G	NP_001305761.1:p.Pro1385Arg
NM_001363528.1:c.4124C>G	NP_001350457.1:p.Pro1375Arg
NM_021055.2:c.4193C>G	NP_066399.2:p.Pro1398Arg
XM_005255531.4:c.4124C>G	XP_005255588.2:p.Pro1375Arg
XM_011522636.2:c.4376C>G	XP_011520938.1:p.Pro1459Arg
XM_011522637.2:c.4373C>G	XP_011520939.1:p.Pro1458Arg
XM_011522638.2:c.4538C>G	XP_011520940.2:p.Pro1513Arg
XM_011522639.2:c.4247C>G	XP_011520941.1:p.Pro1416Arg
XM_011522640.2:c.4244C>G	XP_011520942.1:p.Pro1415Arg
XM_017023615.1:c.4319C>G	XP_016879104.1:p.Pro1440Arg
XM_017023616.1:c.4190C>G	XP_016879105.1:p.Pro1397Arg
XM_017023617.1:c.4286C>G	XP_016879106.1:p.Pro1429Arg
XM_017023618.1:c.3032C>G	XP_016879107.1:p.Pro1011Arg
XM_024450413.1:c.4121C>G	XP_024306181.1:p.Pro1374Arg
NM_000548.5:c.4322C>G MANE Select	NP_000539.2:p.Pro1441Arg
NM_001370404.1:c.4190C>G	NP_001357333.1:p.Pro1397Arg
NM_001370405.1:c.4193C>G	NP_001357334.1:p.Pro1398Arg
NM_001077183.3:c.4121C>G	NP_001070651.1:p.Pro1374Arg
NM_001114382.3:c.4253C>G	NP_001107854.1:p.Pro1418Arg
NM_001318827.2:c.4013C>G	NP_001305756.1:p.Pro1338Arg
NM_001318829.2:c.3977C>G	NP_001305758.1:p.Pro1326Arg
NM_001318831.2:c.3590C>G	NP_001305760.1:p.Pro1197Arg
NM_001318832.2:c.4154C>G	NP_001305761.1:p.Pro1385Arg
NM_001363528.2:c.4124C>G	NP_001350457.1:p.Pro1375Arg
NM_021055.3:c.4193C>G	NP_066399.2:p.Pro1398Arg