Canonical Allele Identifier: CA1482666203
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105185203_105185207delinsTTGTC , CM000666.2:g.105185203_105185207delinsTTGTC GRCh38
NC_000004.11:g.106106360_106106364delinsTTGTC , CM000666.1:g.106106360_106106364delinsTTGTC GRCh37
NC_000004.10:g.106325809_106325813delinsTTGTC NCBI36
NG_028191.1:g.44329_44333delinsTTGTC , LRG_626:g.44329_44333delinsTTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380013.9:c.-192-5157_-192-5153delinsTTGTC (TET2) MANE Select ENSP00000369351.4:n.-192-5157_-192-5153delinsTTGTC
ENST00000265149.9:c.-192-5157_-192-5153delinsTTGTC (TET2) ENSP00000265149.5:n.-192-5157_-192-5153delinsTTGTC
ENST00000305737.6:c.-192-5157_-192-5153delinsTTGTC (TET2) ENSP00000306705.2:n.-192-5157_-192-5153delinsTTGTC
ENST00000380013.8:c.-192-5157_-192-5153delinsTTGTC (TET2) ENSP00000369351.4:n.-192-5157_-192-5153delinsTTGTC
ENST00000394764.2:c.-47+38224_-47+38228delinsTTGTC (TET2) ENSP00000378245.2:n.-47+38224_-47+38228delinsTTGTC
ENST00000413648.2:c.-47+38224_-47+38228delinsTTGTC (TET2) ENSP00000391448.2:n.-47+38224_-47+38228delinsTTGTC
ENST00000504042.5:n.103-5157_103-5153delinsTTGTC (TET2)
ENST00000505801.1:n.48-5157_48-5153delinsTTGTC (TET2)
ENST00000513237.5:c.-110-5157_-110-5153delinsTTGTC (TET2) ENSP00000425443.1:n.-110-5157_-110-5153delinsTTGTC
ENST00000514870.1:c.-192-5157_-192-5153delinsTTGTC (TET2) ENSP00000426885.1:n.-192-5157_-192-5153delinsTTGTC
ENST00000540549.5:c.-173-5157_-173-5153delinsTTGTC (TET2) ENSP00000442788.1:n.-173-5157_-173-5153delinsTTGTC
NM_001127208.2:c.-192-5157_-192-5153delinsTTGTC , LRG_626t1:c.-192-5157_-192-5153delinsTTGTC (TET2) NP_001120680.1:n.-192-5157_-192-5153delinsTTGTC
NM_017628.4:c.-192-5157_-192-5153delinsTTGTC , LRG_626t2:c.-192-5157_-192-5153delinsTTGTC (TET2) NP_060098.3:n.-192-5157_-192-5153delinsTTGTC
NR_126420.1:n.319-7535_319-7531delinsGACAA (TET2-AS1)
XM_005263082.1:c.-47+38224_-47+38228delinsTTGTC (TET2) XP_005263139.1:n.-47+38224_-47+38228delinsTTGTC
XM_006714242.2:c.-192-5157_-192-5153delinsTTGTC (TET2) XP_006714305.1:n.-192-5157_-192-5153delinsTTGTC
XM_011532043.1:c.-192-5157_-192-5153delinsTTGTC (TET2) XP_011530345.1:n.-192-5157_-192-5153delinsTTGTC
XR_244633.2:n.105-5157_105-5153delinsTTGTC (TET2)
XR_244634.2:n.105-5157_105-5153delinsTTGTC (TET2)
XR_427546.2:n.105-5157_105-5153delinsTTGTC (TET2)
XR_938746.1:n.105-5157_105-5153delinsTTGTC (TET2)
XR_938747.1:n.105-5157_105-5153delinsTTGTC (TET2)
XM_005263082.3:c.-47+38224_-47+38228delinsTTGTC (TET2) XP_005263139.1:n.-47+38224_-47+38228delinsTTGTC
XM_006714242.3:c.-192-5157_-192-5153delinsTTGTC (TET2) XP_006714305.1:n.-192-5157_-192-5153delinsTTGTC
XM_017008319.1:c.-192-5157_-192-5153delinsTTGTC (TET2) XP_016863808.1:n.-192-5157_-192-5153delinsTTGTC
XM_024454102.1:c.-192-5157_-192-5153delinsTTGTC (TET2) XP_024309870.1:n.-192-5157_-192-5153delinsTTGTC
XM_024454103.1:c.-192-5157_-192-5153delinsTTGTC (TET2) XP_024309871.1:n.-192-5157_-192-5153delinsTTGTC
XR_001741246.1:n.140-5157_140-5153delinsTTGTC (TET2)
XR_244633.3:n.140-5157_140-5153delinsTTGTC (TET2)
XR_427546.4:n.140-5157_140-5153delinsTTGTC (TET2)
XR_938746.2:n.140-5157_140-5153delinsTTGTC (TET2)
XR_938747.3:n.140-5157_140-5153delinsTTGTC (TET2)
NM_001127208.3:c.-192-5157_-192-5153delinsTTGTC (TET2) MANE Select NP_001120680.1:n.-192-5157_-192-5153delinsTTGTC