Canonical Allele Identifier: CA891843877

Gene: TSC2

Linked Data

• ClinVar Variation Id: 578093
• ClinVar RCV Id: RCV000701005
• dbSNP Id: rs1567498041
• MyVariant Identifiers: chr16:g.2129334del (hg19) ; chr16:g.2079333del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2079333del , CM000678.2:g.2079333del	GRCh38
NC_000016.9:g.2129334del , CM000678.1:g.2129334del	GRCh37
NC_000016.8:g.2069335del	NCBI36
NG_005895.1:g.35028del , LRG_487:g.35028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*1607del	ENSP00000455997.2:n.*1607del
ENST00000642206.2:c.3105del	ENSP00000495146.2:p.Asn1036ThrfsTer6
ENST00000642365.2:c.3186del	ENSP00000495459.2:p.Asn1063ThrfsTer6
ENST00000644417.2:c.*3638del	ENSP00000493912.2:n.*3638del
ENST00000646464.2:c.*4111del	ENSP00000496610.2:n.*4111del
ENST00000219476.9:c.3189del MANE Select	ENSP00000219476.3:p.Asn1064ThrfsTer6
ENST00000350773.9:c.3189del	ENSP00000344383.4:p.Asn1064ThrfsTer6
ENST00000401874.7:c.3057del	ENSP00000384468.2:p.Asn1020ThrfsTer6
ENST00000471143.6:c.417del	ENSP00000458541.2:n.417del
ENST00000568366.6:n.546del
ENST00000568454.6:c.3090del	ENSP00000454487.1:p.Asn1031ThrfsTer6
ENST00000642365.1:c.1843del
ENST00000642561.1:c.3060del	ENSP00000495099.1:p.Asn1021ThrfsTer6
ENST00000642797.1:c.3060del	ENSP00000493846.1:p.Asn1021ThrfsTer6
ENST00000642936.1:c.3057del	ENSP00000494514.1:p.Asn1020ThrfsTer6
ENST00000643088.1:c.3057del	ENSP00000494747.1:p.Asn1020ThrfsTer6
ENST00000643946.1:c.3189del	ENSP00000495927.1:p.Asn1064ThrfsTer6
ENST00000644043.1:c.3060del	ENSP00000496262.1:p.Asn1021ThrfsTer6
ENST00000644329.1:c.3057del	ENSP00000496611.1:p.Asn1020ThrfsTer6
ENST00000644335.1:c.3060del	ENSP00000496317.1:p.Asn1021ThrfsTer6
ENST00000644399.1:c.3179del
ENST00000644722.1:n.335del
ENST00000645024.1:n.1342del
ENST00000646388.1:c.3189del	ENSP00000495921.1:p.Asn1064ThrfsTer6
ENST00000646634.1:n.2073del
ENST00000647042.1:n.481del
ENST00000219476.7:c.3189del	ENSP00000219476.3:p.Asn1064ThrfsTer6
ENST00000350773.8:c.3189del	ENSP00000344383.4:p.Asn1064ThrfsTer6
ENST00000382538.10:c.2913del	ENSP00000371978.6:p.Asn972ThrfsTer6
ENST00000401874.6:c.3057del	ENSP00000384468.2:p.Asn1020ThrfsTer6
ENST00000439117.6:c.*2356del	ENSP00000406980.2:n.*2356del
ENST00000439673.6:c.2949del	ENSP00000399232.2:p.Asn984ThrfsTer6
ENST00000471143.5:c.415del
ENST00000483020.5:c.429del	ENSP00000460310.1:n.429del
ENST00000497886.5:n.1016del
ENST00000561695.1:n.414del
ENST00000568366.5:n.546del
ENST00000568454.5:c.3090del	ENSP00000454487.1:p.Asn1031ThrfsTer6
NM_000548.3:c.3189del , LRG_487t1:c.3189del	NP_000539.2:p.Asn1064ThrfsTer6
NM_001077183.1:c.3057del	NP_001070651.1:p.Asn1020ThrfsTer6
NM_001114382.1:c.3189del	NP_001107854.1:p.Asn1064ThrfsTer6
XM_005255529.3:c.3060del	XP_005255586.2:p.Asn1021ThrfsTer6
XM_005255531.3:c.3060del	XP_005255588.2:p.Asn1021ThrfsTer6
XM_011522636.1:c.3189del	XP_011520938.1:p.Asn1064ThrfsTer6
XM_011522637.1:c.3186del	XP_011520939.1:p.Asn1063ThrfsTer6
XM_011522638.1:c.3078del	XP_011520940.1:p.Asn1027ThrfsTer6
XM_011522639.1:c.3060del	XP_011520941.1:p.Asn1021ThrfsTer6
XM_011522640.1:c.3057del	XP_011520942.1:p.Asn1020ThrfsTer6
XM_011522641.1:c.2949del	XP_011520943.1:p.Asn984ThrfsTer6
NM_000548.4:c.3189del	NP_000539.2:p.Asn1064ThrfsTer6
NM_001077183.2:c.3057del	NP_001070651.1:p.Asn1020ThrfsTer6
NM_001114382.2:c.3189del	NP_001107854.1:p.Asn1064ThrfsTer6
NM_001318827.1:c.2949del	NP_001305756.1:p.Asn984ThrfsTer6
NM_001318829.1:c.2913del	NP_001305758.1:p.Asn972ThrfsTer6
NM_001318831.1:c.2457del	NP_001305760.1:p.Asn820ThrfsTer6
NM_001318832.1:c.3090del	NP_001305761.1:p.Asn1031ThrfsTer6
NM_001363528.1:c.3060del	NP_001350457.1:p.Asn1021ThrfsTer6
NM_021055.2:c.3060del	NP_066399.2:p.Asn1021ThrfsTer6
XM_005255531.4:c.3060del	XP_005255588.2:p.Asn1021ThrfsTer6
XM_011522636.2:c.3189del	XP_011520938.1:p.Asn1064ThrfsTer6
XM_011522637.2:c.3186del	XP_011520939.1:p.Asn1063ThrfsTer6
XM_011522638.2:c.3351del	XP_011520940.2:p.Asn1118ThrfsTer6
XM_011522639.2:c.3060del	XP_011520941.1:p.Asn1021ThrfsTer6
XM_011522640.2:c.3057del	XP_011520942.1:p.Asn1020ThrfsTer6
XM_017023615.1:c.3186del	XP_016879104.1:p.Asn1063ThrfsTer6
XM_017023616.1:c.3057del	XP_016879105.1:p.Asn1020ThrfsTer6
XM_017023617.1:c.3222del	XP_016879106.1:p.Asn1075ThrfsTer6
XM_017023618.1:c.1845del	XP_016879107.1:p.Asn616ThrfsTer6
XM_024450413.1:c.3057del	XP_024306181.1:p.Asn1020ThrfsTer6
NM_000548.5:c.3189del MANE Select	NP_000539.2:p.Asn1064ThrfsTer6
NM_001370404.1:c.3057del	NP_001357333.1:p.Asn1020ThrfsTer6
NM_001370405.1:c.3060del	NP_001357334.1:p.Asn1021ThrfsTer6
NM_001077183.3:c.3057del	NP_001070651.1:p.Asn1020ThrfsTer6
NM_001114382.3:c.3189del	NP_001107854.1:p.Asn1064ThrfsTer6
NM_001318827.2:c.2949del	NP_001305756.1:p.Asn984ThrfsTer6
NM_001318829.2:c.2913del	NP_001305758.1:p.Asn972ThrfsTer6
NM_001318831.2:c.2457del	NP_001305760.1:p.Asn820ThrfsTer6
NM_001318832.2:c.3090del	NP_001305761.1:p.Asn1031ThrfsTer6
NM_001363528.2:c.3060del	NP_001350457.1:p.Asn1021ThrfsTer6
NM_021055.3:c.3060del	NP_066399.2:p.Asn1021ThrfsTer6