Canonical Allele Identifier: CA051555
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs74363455
gnomAD v4: 16-2084998-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084998C>A , CM000678.2:g.2084998C>A GRCh38
NC_000016.9:g.2134999C>A , CM000678.1:g.2134999C>A GRCh37
NC_000016.8:g.2075000C>A NCBI36
NG_005895.1:g.40693C>A , LRG_487:g.40693C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*2890C>A ENSP00000455997.2:n.*2890C>A
ENST00000642206.2:c.4388C>A ENSP00000495146.2:p.Ser1463Ter
ENST00000642365.2:c.4538C>A ENSP00000495459.2:p.Ser1513Ter
ENST00000644417.2:c.*4921C>A ENSP00000493912.2:n.*4921C>A
ENST00000646464.2:c.*7290C>A ENSP00000496610.2:n.*7290C>A
ENST00000219476.9:c.4541C>A MANE Select ENSP00000219476.3:p.Ser1514Ter
ENST00000350773.9:c.4472C>A ENSP00000344383.4:p.Ser1491Ter
ENST00000401874.7:c.4340C>A ENSP00000384468.2:p.Ser1447Ter
ENST00000568454.6:c.4373C>A ENSP00000454487.1:p.Ser1458Ter
ENST00000569110.2:c.764C>A
ENST00000569930.2:n.2423C>A
ENST00000642365.1:c.3195C>A
ENST00000642561.1:c.4412C>A ENSP00000495099.1:p.Ser1471Ter
ENST00000642728.1:n.723C>A
ENST00000642797.1:c.4343C>A ENSP00000493846.1:p.Ser1448Ter
ENST00000642936.1:c.4409C>A ENSP00000494514.1:p.Ser1470Ter
ENST00000643088.1:c.4340C>A ENSP00000494747.1:p.Ser1447Ter
ENST00000643177.1:n.555C>A
ENST00000643426.1:n.2189C>A
ENST00000643946.1:c.4472C>A ENSP00000495927.1:p.Ser1491Ter
ENST00000644043.1:c.4412C>A ENSP00000496262.1:p.Ser1471Ter
ENST00000644329.1:c.4340C>A ENSP00000496611.1:p.Ser1447Ter
ENST00000644335.1:c.4343C>A ENSP00000496317.1:p.Ser1448Ter
ENST00000644399.1:c.4462C>A
ENST00000645024.1:n.2625C>A
ENST00000646388.1:c.4541C>A ENSP00000495921.1:p.Ser1514Ter
ENST00000646634.1:n.3356C>A
ENST00000646674.1:n.1793C>A
ENST00000647042.1:n.1764C>A
ENST00000647180.1:n.1654C>A
ENST00000219476.7:c.4541C>A ENSP00000219476.3:p.Ser1514Ter
ENST00000350773.8:c.4472C>A ENSP00000344383.4:p.Ser1491Ter
ENST00000382538.10:c.4196C>A ENSP00000371978.6:p.Ser1399Ter
ENST00000401874.6:c.4340C>A ENSP00000384468.2:p.Ser1447Ter
ENST00000439117.6:c.*3708C>A ENSP00000406980.2:n.*3708C>A
ENST00000439673.6:c.4232C>A ENSP00000399232.2:p.Ser1411Ter
ENST00000497886.5:n.2299C>A
ENST00000568454.5:c.4373C>A ENSP00000454487.1:p.Ser1458Ter
ENST00000569110.1:c.723C>A
ENST00000569930.1:n.1656C>A
NM_000548.3:c.4541C>A , LRG_487t1:c.4541C>A NP_000539.2:p.Ser1514Ter
NM_001077183.1:c.4340C>A NP_001070651.1:p.Ser1447Ter
NM_001114382.1:c.4472C>A NP_001107854.1:p.Ser1491Ter
XM_005255529.3:c.4412C>A XP_005255586.2:p.Ser1471Ter
XM_005255531.3:c.4343C>A XP_005255588.2:p.Ser1448Ter
XM_011522636.1:c.4595C>A XP_011520938.1:p.Ser1532Ter
XM_011522637.1:c.4592C>A XP_011520939.1:p.Ser1531Ter
XM_011522638.1:c.4484C>A XP_011520940.1:p.Ser1495Ter
XM_011522639.1:c.4466C>A XP_011520941.1:p.Ser1489Ter
XM_011522640.1:c.4463C>A XP_011520942.1:p.Ser1488Ter
XM_011522641.1:c.4232C>A XP_011520943.1:p.Ser1411Ter
NM_000548.4:c.4541C>A NP_000539.2:p.Ser1514Ter
NM_001077183.2:c.4340C>A NP_001070651.1:p.Ser1447Ter
NM_001114382.2:c.4472C>A NP_001107854.1:p.Ser1491Ter
NM_001318827.1:c.4232C>A NP_001305756.1:p.Ser1411Ter
NM_001318829.1:c.4196C>A NP_001305758.1:p.Ser1399Ter
NM_001318831.1:c.3809C>A NP_001305760.1:p.Ser1270Ter
NM_001318832.1:c.4373C>A NP_001305761.1:p.Ser1458Ter
NM_001363528.1:c.4343C>A NP_001350457.1:p.Ser1448Ter
NM_021055.2:c.4412C>A NP_066399.2:p.Ser1471Ter
XM_005255531.4:c.4343C>A XP_005255588.2:p.Ser1448Ter
XM_011522636.2:c.4595C>A XP_011520938.1:p.Ser1532Ter
XM_011522637.2:c.4592C>A XP_011520939.1:p.Ser1531Ter
XM_011522638.2:c.4757C>A XP_011520940.2:p.Ser1586Ter
XM_011522639.2:c.4466C>A XP_011520941.1:p.Ser1489Ter
XM_011522640.2:c.4463C>A XP_011520942.1:p.Ser1488Ter
XM_017023615.1:c.4538C>A XP_016879104.1:p.Ser1513Ter
XM_017023616.1:c.4409C>A XP_016879105.1:p.Ser1470Ter
XM_017023617.1:c.4505C>A XP_016879106.1:p.Ser1502Ter
XM_017023618.1:c.3251C>A XP_016879107.1:p.Ser1084Ter
XM_024450413.1:c.4340C>A XP_024306181.1:p.Ser1447Ter
NM_000548.5:c.4541C>A MANE Select NP_000539.2:p.Ser1514Ter
NM_001370404.1:c.4409C>A NP_001357333.1:p.Ser1470Ter
NM_001370405.1:c.4412C>A NP_001357334.1:p.Ser1471Ter
NM_001077183.3:c.4340C>A NP_001070651.1:p.Ser1447Ter
NM_001114382.3:c.4472C>A NP_001107854.1:p.Ser1491Ter
NM_001318827.2:c.4232C>A NP_001305756.1:p.Ser1411Ter
NM_001318829.2:c.4196C>A NP_001305758.1:p.Ser1399Ter
NM_001318831.2:c.3809C>A NP_001305760.1:p.Ser1270Ter
NM_001318832.2:c.4373C>A NP_001305761.1:p.Ser1458Ter
NM_001363528.2:c.4343C>A NP_001350457.1:p.Ser1448Ter
NM_021055.3:c.4412C>A NP_066399.2:p.Ser1471Ter