Canonical Allele Identifier: CA2580090913
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109777
ClinVar RCV Id: RCV003020077

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2079000_2079170del , CM000678.2:g.2079000_2079170del GRCh38
NC_000016.9:g.2129001_2129171del , CM000678.1:g.2129001_2129171del GRCh37
NC_000016.8:g.2069002_2069172del NCBI36
NG_005895.1:g.34695_34865del , LRG_487:g.34695_34865del

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*1385-32_*1523del
ENST00000642206.2:c.2883-32_3021del
ENST00000642365.2:c.2967-35_3102del
ENST00000644417.2:c.*3416-32_*3554del
ENST00000646464.2:c.*3892-35_*4027del
ENST00000219476.9:c.2967-32_3105del
ENST00000350773.9:c.2967-32_3105del
ENST00000401874.7:c.2838-35_2973del
ENST00000471143.6:c.198-35_333del
ENST00000568366.6:n.324-32_462del
ENST00000568454.6:c.2871-35_3006del
ENST00000642365.1:c.1624-35_1759del
ENST00000642561.1:c.2838-32_2976del
ENST00000642797.1:c.2838-32_2976del
ENST00000642936.1:c.2838-35_2973del
ENST00000643088.1:c.2838-35_2973del
ENST00000643946.1:c.2967-32_3105del
ENST00000644043.1:c.2838-32_2976del
ENST00000644329.1:c.2838-35_2973del
ENST00000644335.1:c.2838-32_2976del
ENST00000644399.1:c.2960-35_3095del
ENST00000644722.1:n.81_251del
ENST00000645024.1:n.1120-32_1258del
ENST00000646388.1:c.2967-32_3105del
ENST00000646634.1:n.1851-32_1989del
ENST00000647042.1:n.227_397del
ENST00000219476.7:c.2967-32_3105del
ENST00000350773.8:c.2967-32_3105del
ENST00000382538.10:c.2691-32_2829del
ENST00000401874.6:c.2838-35_2973del
ENST00000439117.6:c.*2137-35_*2272del
ENST00000439673.6:c.2727-32_2865del
ENST00000471143.5:c.196-35_331del
ENST00000483020.5:c.207-32_345del
ENST00000497886.5:n.762_932del
ENST00000561695.1:n.81_251del
ENST00000568366.5:n.324-32_462del
ENST00000568454.5:c.2871-35_3006del
NM_000548.3:c.2967-32_3105del , LRG_487t1:c.2967-32_3105del
NM_001077183.1:c.2838-35_2973del
NM_001114382.1:c.2967-32_3105del
XM_005255529.3:c.2838-32_2976del
XM_005255531.3:c.2838-32_2976del
XM_011522636.1:c.2967-32_3105del
XM_011522637.1:c.2967-35_3102del
XM_011522638.1:c.2856-32_2994del
XM_011522639.1:c.2838-32_2976del
XM_011522640.1:c.2838-35_2973del
XM_011522641.1:c.2727-32_2865del
NM_000548.4:c.2967-32_3105del
NM_001077183.2:c.2838-35_2973del
NM_001114382.2:c.2967-32_3105del
NM_001318827.1:c.2727-32_2865del
NM_001318829.1:c.2691-32_2829del
NM_001318831.1:c.2238-35_2373del
NM_001318832.1:c.2871-35_3006del
NM_001363528.1:c.2838-32_2976del
NM_021055.2:c.2838-32_2976del
XM_005255531.4:c.2838-32_2976del
XM_011522636.2:c.2967-32_3105del
XM_011522637.2:c.2967-35_3102del
XM_011522638.2:c.3129-32_3267del
XM_011522639.2:c.2838-32_2976del
XM_011522640.2:c.2838-35_2973del
XM_017023615.1:c.2967-35_3102del
XM_017023616.1:c.2838-35_2973del
XM_017023617.1:c.3000-32_3138del
XM_017023618.1:c.1623-32_1761del
XM_024450413.1:c.2838-35_2973del
NM_000548.5:c.2967-32_3105del
NM_001370404.1:c.2838-35_2973del
NM_001370405.1:c.2838-32_2976del
NM_001077183.3:c.2838-35_2973del
NM_001114382.3:c.2967-32_3105del
NM_001318827.2:c.2727-32_2865del
NM_001318829.2:c.2691-32_2829del
NM_001318831.2:c.2238-35_2373del
NM_001318832.2:c.2871-35_3006del
NM_001363528.2:c.2838-32_2976del
NM_021055.3:c.2838-32_2976del