Canonical Allele Identifier: CA017760

Gene: TSC2

Linked Data

• ClinVar Variation Id: 49845
• ClinVar RCV Id: RCV000043111 ; RCV000201066
• dbSNP Id: rs45517252
• MyVariant Identifiers: chr16:g.2125894G>C (hg19) ; chr16:g.2075893G>C (hg38)
• PubMed: PMID:11112665 ; PMID:16981987

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2075893G>C , CM000678.2:g.2075893G>C	GRCh38
NC_000016.9:g.2125894G>C , CM000678.1:g.2125894G>C	GRCh37
NC_000016.8:g.2065895G>C	NCBI36
NG_005895.1:g.31588G>C , LRG_487:g.31588G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*1186+1G>C	ENSP00000455997.2:n.*1186+1G>C
ENST00000642206.2:c.2684+1G>C	ENSP00000495146.2:n.2684+1G>C
ENST00000642365.2:c.2639+1G>C	ENSP00000495459.2:n.2639+1G>C
ENST00000644417.2:c.*2076+1G>C	ENSP00000493912.2:n.*2076+1G>C
ENST00000646464.2:c.*3693+1G>C	ENSP00000496610.2:n.*3693+1G>C
ENST00000219476.9:c.2639+1G>C MANE Select	ENSP00000219476.3:n.2639+1G>C
ENST00000350773.9:c.2639+1G>C	ENSP00000344383.4:n.2639+1G>C
ENST00000401874.7:c.2639+1G>C	ENSP00000384468.2:n.2639+1G>C
ENST00000568454.6:c.2672+1G>C	ENSP00000454487.1:n.2672+1G>C
ENST00000642365.1:c.1296+1G>C
ENST00000642561.1:c.2639+1G>C	ENSP00000495099.1:n.2639+1G>C
ENST00000642797.1:c.2639+1G>C	ENSP00000493846.1:n.2639+1G>C
ENST00000642936.1:c.2639+1G>C	ENSP00000494514.1:n.2639+1G>C
ENST00000643088.1:c.2639+1G>C	ENSP00000494747.1:n.2639+1G>C
ENST00000643298.1:c.*2141+1G>C	ENSP00000494393.1:n.*2141+1G>C
ENST00000643946.1:c.2639+1G>C	ENSP00000495927.1:n.2639+1G>C
ENST00000644043.1:c.2639+1G>C	ENSP00000496262.1:n.2639+1G>C
ENST00000644329.1:c.2639+1G>C	ENSP00000496611.1:n.2639+1G>C
ENST00000644335.1:c.2639+1G>C	ENSP00000496317.1:n.2639+1G>C
ENST00000644399.1:c.2632+1G>C
ENST00000645024.1:n.921+1G>C
ENST00000646388.1:c.2639+1G>C	ENSP00000495921.1:n.2639+1G>C
ENST00000646634.1:n.1652+1G>C
ENST00000219476.7:c.2639+1G>C	ENSP00000219476.3:n.2639+1G>C
ENST00000350773.8:c.2639+1G>C	ENSP00000344383.4:n.2639+1G>C
ENST00000382538.10:c.2492+1G>C	ENSP00000371978.6:n.2492+1G>C
ENST00000401874.6:c.2639+1G>C	ENSP00000384468.2:n.2639+1G>C
ENST00000439117.6:c.*1938+1G>C	ENSP00000406980.2:n.*1938+1G>C
ENST00000439673.6:c.2528+1G>C	ENSP00000399232.2:n.2528+1G>C
ENST00000568454.5:c.2672+1G>C	ENSP00000454487.1:n.2672+1G>C
NM_000548.3:c.2639+1G>C , LRG_487t1:c.2639+1G>C	NP_000539.2:n.2639+1G>C
NM_001077183.1:c.2639+1G>C	NP_001070651.1:n.2639+1G>C
NM_001114382.1:c.2639+1G>C	NP_001107854.1:n.2639+1G>C
XM_005255529.3:c.2639+1G>C	XP_005255586.2:n.2639+1G>C
XM_005255531.3:c.2639+1G>C	XP_005255588.2:n.2639+1G>C
XM_011522636.1:c.2639+1G>C	XP_011520938.1:n.2639+1G>C
XM_011522637.1:c.2639+1G>C	XP_011520939.1:n.2639+1G>C
XM_011522638.1:c.2528+1G>C	XP_011520940.1:n.2528+1G>C
XM_011522639.1:c.2639+1G>C	XP_011520941.1:n.2639+1G>C
XM_011522640.1:c.2639+1G>C	XP_011520942.1:n.2639+1G>C
XM_011522641.1:c.2528+1G>C	XP_011520943.1:n.2528+1G>C
NM_000548.4:c.2639+1G>C	NP_000539.2:n.2639+1G>C
NM_001077183.2:c.2639+1G>C	NP_001070651.1:n.2639+1G>C
NM_001114382.2:c.2639+1G>C	NP_001107854.1:n.2639+1G>C
NM_001318827.1:c.2528+1G>C	NP_001305756.1:n.2528+1G>C
NM_001318829.1:c.2492+1G>C	NP_001305758.1:n.2492+1G>C
NM_001318831.1:c.2039+1G>C	NP_001305760.1:n.2039+1G>C
NM_001318832.1:c.2672+1G>C	NP_001305761.1:n.2672+1G>C
NM_001363528.1:c.2639+1G>C	NP_001350457.1:n.2639+1G>C
NM_021055.2:c.2639+1G>C	NP_066399.2:n.2639+1G>C
XM_005255531.4:c.2639+1G>C	XP_005255588.2:n.2639+1G>C
XM_011522636.2:c.2639+1G>C	XP_011520938.1:n.2639+1G>C
XM_011522637.2:c.2639+1G>C	XP_011520939.1:n.2639+1G>C
XM_011522638.2:c.2801+1G>C	XP_011520940.2:n.2801+1G>C
XM_011522639.2:c.2639+1G>C	XP_011520941.1:n.2639+1G>C
XM_011522640.2:c.2639+1G>C	XP_011520942.1:n.2639+1G>C
XM_017023615.1:c.2639+1G>C	XP_016879104.1:n.2639+1G>C
XM_017023616.1:c.2639+1G>C	XP_016879105.1:n.2639+1G>C
XM_017023617.1:c.2801+1G>C	XP_016879106.1:n.2801+1G>C
XM_017023618.1:c.1295+1G>C	XP_016879107.1:n.1295+1G>C
XM_024450413.1:c.2639+1G>C	XP_024306181.1:n.2639+1G>C
NM_000548.5:c.2639+1G>C MANE Select	NP_000539.2:n.2639+1G>C
NM_001370404.1:c.2639+1G>C	NP_001357333.1:n.2639+1G>C
NM_001370405.1:c.2639+1G>C	NP_001357334.1:n.2639+1G>C
NM_001077183.3:c.2639+1G>C	NP_001070651.1:n.2639+1G>C
NM_001114382.3:c.2639+1G>C	NP_001107854.1:n.2639+1G>C
NM_001318827.2:c.2528+1G>C	NP_001305756.1:n.2528+1G>C
NM_001318829.2:c.2492+1G>C	NP_001305758.1:n.2492+1G>C
NM_001318831.2:c.2039+1G>C	NP_001305760.1:n.2039+1G>C
NM_001318832.2:c.2672+1G>C	NP_001305761.1:n.2672+1G>C
NM_001363528.2:c.2639+1G>C	NP_001350457.1:n.2639+1G>C
NM_021055.3:c.2639+1G>C	NP_066399.2:n.2639+1G>C