Canonical Allele Identifier: CA394292351
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050887
ClinVar RCV Id: RCV001358846
dbSNP Id: rs938124834

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2081666C>A , CM000678.2:g.2081666C>A GRCh38
NC_000016.9:g.2131667C>A , CM000678.1:g.2131667C>A GRCh37
NC_000016.8:g.2071668C>A NCBI36
NG_005895.1:g.37361C>A , LRG_487:g.37361C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2100C>A ENSP00000455997.2:n.*2100C>A
ENST00000642206.2:c.3598C>A ENSP00000495146.2:p.Leu1200Met
ENST00000642365.2:c.3679C>A ENSP00000495459.2:p.Leu1227Met
ENST00000644417.2:c.*4131C>A ENSP00000493912.2:n.*4131C>A
ENST00000646464.2:c.*4604C>A ENSP00000496610.2:n.*4604C>A
ENST00000219476.9:c.3682C>A MANE Select ENSP00000219476.3:p.Leu1228Met
ENST00000350773.9:c.3682C>A ENSP00000344383.4:p.Leu1228Met
ENST00000401874.7:c.3550C>A ENSP00000384468.2:p.Leu1184Met
ENST00000568454.6:c.3583C>A ENSP00000454487.1:p.Leu1195Met
ENST00000642365.1:c.2336C>A
ENST00000642561.1:c.3553C>A ENSP00000495099.1:p.Leu1185Met
ENST00000642797.1:c.3553C>A ENSP00000493846.1:p.Leu1185Met
ENST00000642936.1:c.3550C>A ENSP00000494514.1:p.Leu1184Met
ENST00000643088.1:c.3550C>A ENSP00000494747.1:p.Leu1184Met
ENST00000643426.1:n.1330C>A
ENST00000643533.1:n.192C>A
ENST00000643946.1:c.3682C>A ENSP00000495927.1:p.Leu1228Met
ENST00000644043.1:c.3553C>A ENSP00000496262.1:p.Leu1185Met
ENST00000644329.1:c.3550C>A ENSP00000496611.1:p.Leu1184Met
ENST00000644335.1:c.3553C>A ENSP00000496317.1:p.Leu1185Met
ENST00000644399.1:c.3672C>A
ENST00000644722.1:n.828C>A
ENST00000645024.1:n.1835C>A
ENST00000646388.1:c.3682C>A ENSP00000495921.1:p.Leu1228Met
ENST00000646634.1:n.2566C>A
ENST00000646674.1:n.297C>A
ENST00000647042.1:n.974C>A
ENST00000647180.1:n.162C>A
ENST00000219476.7:c.3682C>A ENSP00000219476.3:p.Leu1228Met
ENST00000350773.8:c.3682C>A ENSP00000344383.4:p.Leu1228Met
ENST00000382538.10:c.3406C>A ENSP00000371978.6:p.Leu1136Met
ENST00000401874.6:c.3550C>A ENSP00000384468.2:p.Leu1184Met
ENST00000439117.6:c.*2849C>A ENSP00000406980.2:n.*2849C>A
ENST00000439673.6:c.3442C>A ENSP00000399232.2:p.Leu1148Met
ENST00000497886.5:n.1509C>A
ENST00000568454.5:c.3583C>A ENSP00000454487.1:p.Leu1195Met
NM_000548.3:c.3682C>A , LRG_487t1:c.3682C>A NP_000539.2:p.Leu1228Met
NM_001077183.1:c.3550C>A NP_001070651.1:p.Leu1184Met
NM_001114382.1:c.3682C>A NP_001107854.1:p.Leu1228Met
XM_005255529.3:c.3553C>A XP_005255586.2:p.Leu1185Met
XM_005255531.3:c.3553C>A XP_005255588.2:p.Leu1185Met
XM_011522636.1:c.3682C>A XP_011520938.1:p.Leu1228Met
XM_011522637.1:c.3679C>A XP_011520939.1:p.Leu1227Met
XM_011522638.1:c.3571C>A XP_011520940.1:p.Leu1191Met
XM_011522639.1:c.3553C>A XP_011520941.1:p.Leu1185Met
XM_011522640.1:c.3550C>A XP_011520942.1:p.Leu1184Met
XM_011522641.1:c.3442C>A XP_011520943.1:p.Leu1148Met
NM_000548.4:c.3682C>A NP_000539.2:p.Leu1228Met
NM_001077183.2:c.3550C>A NP_001070651.1:p.Leu1184Met
NM_001114382.2:c.3682C>A NP_001107854.1:p.Leu1228Met
NM_001318827.1:c.3442C>A NP_001305756.1:p.Leu1148Met
NM_001318829.1:c.3406C>A NP_001305758.1:p.Leu1136Met
NM_001318831.1:c.2950C>A NP_001305760.1:p.Leu984Met
NM_001318832.1:c.3583C>A NP_001305761.1:p.Leu1195Met
NM_001363528.1:c.3553C>A NP_001350457.1:p.Leu1185Met
NM_021055.2:c.3553C>A NP_066399.2:p.Leu1185Met
XM_005255531.4:c.3553C>A XP_005255588.2:p.Leu1185Met
XM_011522636.2:c.3682C>A XP_011520938.1:p.Leu1228Met
XM_011522637.2:c.3679C>A XP_011520939.1:p.Leu1227Met
XM_011522638.2:c.3844C>A XP_011520940.2:p.Leu1282Met
XM_011522639.2:c.3553C>A XP_011520941.1:p.Leu1185Met
XM_011522640.2:c.3550C>A XP_011520942.1:p.Leu1184Met
XM_017023615.1:c.3679C>A XP_016879104.1:p.Leu1227Met
XM_017023616.1:c.3550C>A XP_016879105.1:p.Leu1184Met
XM_017023617.1:c.3715C>A XP_016879106.1:p.Leu1239Met
XM_017023618.1:c.2338C>A XP_016879107.1:p.Leu780Met
XM_024450413.1:c.3550C>A XP_024306181.1:p.Leu1184Met
NM_000548.5:c.3682C>A MANE Select NP_000539.2:p.Leu1228Met
NM_001370404.1:c.3550C>A NP_001357333.1:p.Leu1184Met
NM_001370405.1:c.3553C>A NP_001357334.1:p.Leu1185Met
NM_001077183.3:c.3550C>A NP_001070651.1:p.Leu1184Met
NM_001114382.3:c.3682C>A NP_001107854.1:p.Leu1228Met
NM_001318827.2:c.3442C>A NP_001305756.1:p.Leu1148Met
NM_001318829.2:c.3406C>A NP_001305758.1:p.Leu1136Met
NM_001318831.2:c.2950C>A NP_001305760.1:p.Leu984Met
NM_001318832.2:c.3583C>A NP_001305761.1:p.Leu1195Met
NM_001363528.2:c.3553C>A NP_001350457.1:p.Leu1185Met
NM_021055.3:c.3553C>A NP_066399.2:p.Leu1185Met