Canonical Allele Identifier: CA2571833302
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105185184_105185185insGGGGGGGGGGGGGGGGGGGGGG , CM000666.2:g.105185184_105185185insGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000004.11:g.106106341_106106342insGGGGGGGGGGGGGGGGGGGGGG , CM000666.1:g.106106341_106106342insGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000004.10:g.106325790_106325791insGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_028191.1:g.44310_44311insGGGGGGGGGGGGGGGGGGGGGG , LRG_626:g.44310_44311insGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000380013.9:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) MANE Select ENSP00000369351.4:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGG...
ENST00000265149.9:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000265149.5:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGG...
ENST00000305737.6:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000306705.2:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGG...
ENST00000380013.8:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000369351.4:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGG...
ENST00000394764.2:c.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000378245.2:n.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGG...
ENST00000413648.2:c.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000391448.2:n.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGG...
ENST00000504042.5:n.103-5176_103-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
ENST00000505801.1:n.48-5176_48-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
ENST00000513237.5:c.-110-5176_-110-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000425443.1:n.-110-5176_-110-5175insGGGGGGGGGGGGGGGGGGG...
ENST00000514870.1:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000426885.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGG...
ENST00000540549.5:c.-173-5176_-173-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) ENSP00000442788.1:n.-173-5176_-173-5175insGGGGGGGGGGGGGGGGGGG...
NM_001127208.2:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG , LRG_626t1:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) NP_001120680.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
NM_017628.4:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG , LRG_626t2:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) NP_060098.3:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG
NR_126420.1:n.319-7513_319-7512insCCCCCCCCCCCCCCCCCCCCCC (TET2-AS1)
XM_005263082.1:c.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_005263139.1:n.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGGGGG...
XM_006714242.2:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_006714305.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
XM_011532043.1:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_011530345.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
XR_244633.2:n.105-5176_105-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_244634.2:n.105-5176_105-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_427546.2:n.105-5176_105-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_938746.1:n.105-5176_105-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_938747.1:n.105-5176_105-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XM_005263082.3:c.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_005263139.1:n.-47+38205_-47+38206insGGGGGGGGGGGGGGGGGGGGGG...
XM_006714242.3:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_006714305.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
XM_017008319.1:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_016863808.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
XM_024454102.1:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_024309870.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
XM_024454103.1:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) XP_024309871.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...
XR_001741246.1:n.140-5176_140-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_244633.3:n.140-5176_140-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_427546.4:n.140-5176_140-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_938746.2:n.140-5176_140-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
XR_938747.3:n.140-5176_140-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2)
NM_001127208.3:c.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG (TET2) MANE Select NP_001120680.1:n.-192-5176_-192-5175insGGGGGGGGGGGGGGGGGGGGGG...