Canonical Allele Identifier: CA357811683
Community Standard Title: NM_001127208.3(TET2):c.4393C>T (p.Arg1465Ter)
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105272774C>T , CM000666.2:g.105272774C>T GRCh38
NC_000004.11:g.106193931C>T , CM000666.1:g.106193931C>T GRCh37
NC_000004.10:g.106413380C>T NCBI36
NG_028191.1:g.131900C>T , LRG_626:g.131900C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001127208.3:c.4393C>T (TET2) MANE Select NP_001120680.1:p.Arg1465Ter
ENST00000380013.9:c.4393C>T (TET2) MANE Select ENSP00000369351.4:p.Arg1465Ter
NM_001127208.2:c.4393C>T , LRG_626t1:c.4393C>T (TET2) NP_001120680.1:p.Arg1465Ter
NR_126420.1:n.318+61612G>A (TET2-AS1)
ENST00000265149.9:c.*717C>T (TET2) ENSP00000265149.5:n.*717C>T
ENST00000380013.8:c.4393C>T (TET2) ENSP00000369351.4:p.Arg1465Ter
ENST00000513237.5:c.4456C>T (TET2) ENSP00000425443.1:p.Arg1486Ter
ENST00000540549.5:c.4393C>T (TET2) ENSP00000442788.1:p.Arg1465Ter
XM_005263082.1:c.4393C>T (TET2) XP_005263139.1:p.Arg1465Ter
XM_005263082.3:c.4393C>T (TET2) XP_005263139.1:p.Arg1465Ter
XM_006714242.2:c.4093C>T (TET2) XP_006714305.1:p.Arg1365Ter
XM_006714242.3:c.4093C>T (TET2) XP_006714305.1:p.Arg1365Ter
XM_011532044.1:c.904C>T (TET2) XP_011530346.1:p.Arg302Ter
XM_024454102.1:c.4393C>T (TET2) XP_024309870.1:p.Arg1465Ter
XM_024454103.1:c.4393C>T (TET2) XP_024309871.1:p.Arg1465Ter
XR_244633.2:n.4295C>T (TET2)
XR_244633.3:n.4330C>T (TET2)
XR_244634.2:n.4598C>T (TET2)
XR_427546.4:n.4515C>T (TET2)