Canonical Allele Identifier: CA1482681209
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105218711_105218717delinsGTGTCTA , CM000666.2:g.105218711_105218717delinsGTGTCTA GRCh38
NC_000004.11:g.106139868_106139874delinsGTGTCTA , CM000666.1:g.106139868_106139874delinsGTGTCTA GRCh37
NC_000004.10:g.106359317_106359323delinsGTGTCTA NCBI36
NG_028191.1:g.77837_77843delinsGTGTCTA , LRG_626:g.77837_77843delinsGTGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380013.9:c.-46-15186_-46-15180delinsGTGTCTA (TET2) MANE Select ENSP00000369351.4:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000265149.9:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000265149.5:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000305737.6:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000306705.2:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000380013.8:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000369351.4:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000394764.2:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000378245.2:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000413648.2:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000391448.2:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000513237.5:c.18-15186_18-15180delinsGTGTCTA (TET2) ENSP00000425443.1:n.18-15186_18-15180delinsGTGTCTA
ENST00000514870.1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000426885.1:n.-46-15186_-46-15180delinsGTGTCTA
ENST00000540549.5:c.-46-15186_-46-15180delinsGTGTCTA (TET2) ENSP00000442788.1:n.-46-15186_-46-15180delinsGTGTCTA
NM_001127208.2:c.-46-15186_-46-15180delinsGTGTCTA , LRG_626t1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) NP_001120680.1:n.-46-15186_-46-15180delinsGTGTCTA
NM_017628.4:c.-46-15186_-46-15180delinsGTGTCTA , LRG_626t2:c.-46-15186_-46-15180delinsGTGTCTA (TET2) NP_060098.3:n.-46-15186_-46-15180delinsGTGTCTA
NR_126420.1:n.319-41045_319-41039delinsTAGACAC (TET2-AS1)
XM_005263082.1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_005263139.1:n.-46-15186_-46-15180delinsGTGTCTA
XM_006714242.2:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_006714305.1:n.-46-15186_-46-15180delinsGTGTCTA
XM_011532043.1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_011530345.1:n.-46-15186_-46-15180delinsGTGTCTA
XR_244633.2:n.251-15186_251-15180delinsGTGTCTA (TET2)
XR_244634.2:n.251-15186_251-15180delinsGTGTCTA (TET2)
XR_427546.2:n.251-15186_251-15180delinsGTGTCTA (TET2)
XR_938746.1:n.251-15186_251-15180delinsGTGTCTA (TET2)
XR_938747.1:n.251-15186_251-15180delinsGTGTCTA (TET2)
XM_005263082.3:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_005263139.1:n.-46-15186_-46-15180delinsGTGTCTA
XM_006714242.3:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_006714305.1:n.-46-15186_-46-15180delinsGTGTCTA
XM_017008319.1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_016863808.1:n.-46-15186_-46-15180delinsGTGTCTA
XM_024454102.1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_024309870.1:n.-46-15186_-46-15180delinsGTGTCTA
XM_024454103.1:c.-46-15186_-46-15180delinsGTGTCTA (TET2) XP_024309871.1:n.-46-15186_-46-15180delinsGTGTCTA
XR_001741246.1:n.286-15186_286-15180delinsGTGTCTA (TET2)
XR_244633.3:n.286-15186_286-15180delinsGTGTCTA (TET2)
XR_427546.4:n.286-15186_286-15180delinsGTGTCTA (TET2)
XR_938746.2:n.286-15186_286-15180delinsGTGTCTA (TET2)
XR_938747.3:n.286-15186_286-15180delinsGTGTCTA (TET2)
NM_001127208.3:c.-46-15186_-46-15180delinsGTGTCTA (TET2) MANE Select NP_001120680.1:n.-46-15186_-46-15180delinsGTGTCTA