Canonical Allele Identifier: CA394302926

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2134997G>T (hg19) ; chr16:g.2084996G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084996G>T , CM000678.2:g.2084996G>T	GRCh38
NC_000016.9:g.2134997G>T , CM000678.1:g.2134997G>T	GRCh37
NC_000016.8:g.2074998G>T	NCBI36
NG_005895.1:g.40691G>T , LRG_487:g.40691G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*2888G>T	ENSP00000455997.2:n.*2888G>T
ENST00000642206.2:c.4386G>T	ENSP00000495146.2:p.Glu1462Asp
ENST00000642365.2:c.4536G>T	ENSP00000495459.2:p.Glu1512Asp
ENST00000644417.2:c.*4919G>T	ENSP00000493912.2:n.*4919G>T
ENST00000646464.2:c.*7288G>T	ENSP00000496610.2:n.*7288G>T
ENST00000219476.9:c.4539G>T MANE Select	ENSP00000219476.3:p.Glu1513Asp
ENST00000350773.9:c.4470G>T	ENSP00000344383.4:p.Glu1490Asp
ENST00000401874.7:c.4338G>T	ENSP00000384468.2:p.Glu1446Asp
ENST00000568454.6:c.4371G>T	ENSP00000454487.1:p.Glu1457Asp
ENST00000569110.2:c.762G>T
ENST00000569930.2:n.2421G>T
ENST00000642365.1:c.3193G>T
ENST00000642561.1:c.4410G>T	ENSP00000495099.1:p.Glu1470Asp
ENST00000642728.1:n.721G>T
ENST00000642797.1:c.4341G>T	ENSP00000493846.1:p.Glu1447Asp
ENST00000642936.1:c.4407G>T	ENSP00000494514.1:p.Glu1469Asp
ENST00000643088.1:c.4338G>T	ENSP00000494747.1:p.Glu1446Asp
ENST00000643177.1:n.553G>T
ENST00000643426.1:n.2187G>T
ENST00000643946.1:c.4470G>T	ENSP00000495927.1:p.Glu1490Asp
ENST00000644043.1:c.4410G>T	ENSP00000496262.1:p.Glu1470Asp
ENST00000644329.1:c.4338G>T	ENSP00000496611.1:p.Glu1446Asp
ENST00000644335.1:c.4341G>T	ENSP00000496317.1:p.Glu1447Asp
ENST00000644399.1:c.4460G>T
ENST00000645024.1:n.2623G>T
ENST00000646388.1:c.4539G>T	ENSP00000495921.1:p.Glu1513Asp
ENST00000646634.1:n.3354G>T
ENST00000646674.1:n.1791G>T
ENST00000647042.1:n.1762G>T
ENST00000647180.1:n.1652G>T
ENST00000219476.7:c.4539G>T	ENSP00000219476.3:p.Glu1513Asp
ENST00000350773.8:c.4470G>T	ENSP00000344383.4:p.Glu1490Asp
ENST00000382538.10:c.4194G>T	ENSP00000371978.6:p.Glu1398Asp
ENST00000401874.6:c.4338G>T	ENSP00000384468.2:p.Glu1446Asp
ENST00000439117.6:c.*3706G>T	ENSP00000406980.2:n.*3706G>T
ENST00000439673.6:c.4230G>T	ENSP00000399232.2:p.Glu1410Asp
ENST00000497886.5:n.2297G>T
ENST00000568454.5:c.4371G>T	ENSP00000454487.1:p.Glu1457Asp
ENST00000569110.1:c.721G>T
ENST00000569930.1:n.1654G>T
NM_000548.3:c.4539G>T , LRG_487t1:c.4539G>T	NP_000539.2:p.Glu1513Asp
NM_001077183.1:c.4338G>T	NP_001070651.1:p.Glu1446Asp
NM_001114382.1:c.4470G>T	NP_001107854.1:p.Glu1490Asp
XM_005255529.3:c.4410G>T	XP_005255586.2:p.Glu1470Asp
XM_005255531.3:c.4341G>T	XP_005255588.2:p.Glu1447Asp
XM_011522636.1:c.4593G>T	XP_011520938.1:p.Glu1531Asp
XM_011522637.1:c.4590G>T	XP_011520939.1:p.Glu1530Asp
XM_011522638.1:c.4482G>T	XP_011520940.1:p.Glu1494Asp
XM_011522639.1:c.4464G>T	XP_011520941.1:p.Glu1488Asp
XM_011522640.1:c.4461G>T	XP_011520942.1:p.Glu1487Asp
XM_011522641.1:c.4230G>T	XP_011520943.1:p.Glu1410Asp
NM_000548.4:c.4539G>T	NP_000539.2:p.Glu1513Asp
NM_001077183.2:c.4338G>T	NP_001070651.1:p.Glu1446Asp
NM_001114382.2:c.4470G>T	NP_001107854.1:p.Glu1490Asp
NM_001318827.1:c.4230G>T	NP_001305756.1:p.Glu1410Asp
NM_001318829.1:c.4194G>T	NP_001305758.1:p.Glu1398Asp
NM_001318831.1:c.3807G>T	NP_001305760.1:p.Glu1269Asp
NM_001318832.1:c.4371G>T	NP_001305761.1:p.Glu1457Asp
NM_001363528.1:c.4341G>T	NP_001350457.1:p.Glu1447Asp
NM_021055.2:c.4410G>T	NP_066399.2:p.Glu1470Asp
XM_005255531.4:c.4341G>T	XP_005255588.2:p.Glu1447Asp
XM_011522636.2:c.4593G>T	XP_011520938.1:p.Glu1531Asp
XM_011522637.2:c.4590G>T	XP_011520939.1:p.Glu1530Asp
XM_011522638.2:c.4755G>T	XP_011520940.2:p.Glu1585Asp
XM_011522639.2:c.4464G>T	XP_011520941.1:p.Glu1488Asp
XM_011522640.2:c.4461G>T	XP_011520942.1:p.Glu1487Asp
XM_017023615.1:c.4536G>T	XP_016879104.1:p.Glu1512Asp
XM_017023616.1:c.4407G>T	XP_016879105.1:p.Glu1469Asp
XM_017023617.1:c.4503G>T	XP_016879106.1:p.Glu1501Asp
XM_017023618.1:c.3249G>T	XP_016879107.1:p.Glu1083Asp
XM_024450413.1:c.4338G>T	XP_024306181.1:p.Glu1446Asp
NM_000548.5:c.4539G>T MANE Select	NP_000539.2:p.Glu1513Asp
NM_001370404.1:c.4407G>T	NP_001357333.1:p.Glu1469Asp
NM_001370405.1:c.4410G>T	NP_001357334.1:p.Glu1470Asp
NM_001077183.3:c.4338G>T	NP_001070651.1:p.Glu1446Asp
NM_001114382.3:c.4470G>T	NP_001107854.1:p.Glu1490Asp
NM_001318827.2:c.4230G>T	NP_001305756.1:p.Glu1410Asp
NM_001318829.2:c.4194G>T	NP_001305758.1:p.Glu1398Asp
NM_001318831.2:c.3807G>T	NP_001305760.1:p.Glu1269Asp
NM_001318832.2:c.4371G>T	NP_001305761.1:p.Glu1457Asp
NM_001363528.2:c.4341G>T	NP_001350457.1:p.Glu1447Asp
NM_021055.3:c.4410G>T	NP_066399.2:p.Glu1470Asp