Canonical Allele Identifier: CA1482692451
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105278305A= , CM000666.2:g.105278305A= GRCh38
NC_000004.11:g.106199462A= , CM000666.1:g.106199462A= GRCh37
NC_000004.10:g.106418911A= NCBI36
NG_028191.1:g.137431A= , LRG_626:g.137431A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380013.9:c.*1786A= (TET2) MANE Select ENSP00000369351.4:n.*1786A=
ENST00000265149.9:c.*4119A= (TET2) ENSP00000265149.5:n.*4119A=
ENST00000380013.8:c.*1786A= (TET2) ENSP00000369351.4:n.*1786A=
ENST00000513237.5:c.*1786A= (TET2) ENSP00000425443.1:n.*1786A=
ENST00000540549.5:c.*1786A= (TET2) ENSP00000442788.1:n.*1786A=
NM_001127208.2:c.*1786A= , LRG_626t1:c.*1786A= (TET2) NP_001120680.1:n.*1786A=
NR_126420.1:n.318+56081T= (TET2-AS1)
XM_005263082.1:c.*1786A= (TET2) XP_005263139.1:n.*1786A=
XM_006714242.2:c.*1786A= (TET2) XP_006714305.1:n.*1786A=
XM_011532044.1:c.*1786A= (TET2) XP_011530346.1:n.*1786A=
XR_244633.2:n.7697A= (TET2)
XR_244634.2:n.8000A= (TET2)
XM_005263082.3:c.*1786A= (TET2) XP_005263139.1:n.*1786A=
XM_006714242.3:c.*1786A= (TET2) XP_006714305.1:n.*1786A=
XM_024454102.1:c.*1786A= (TET2) XP_024309870.1:n.*1786A=
XM_024454103.1:c.*1786A= (TET2) XP_024309871.1:n.*1786A=
XR_244633.3:n.7732A= (TET2)
NM_001127208.3:c.*1786A= (TET2) MANE Select NP_001120680.1:n.*1786A=