Canonical Allele Identifier: CA553594608
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1483517861

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105218219_105218221del , CM000666.2:g.105218219_105218221del GRCh38
NC_000004.11:g.106139376_106139378del , CM000666.1:g.106139376_106139378del GRCh37
NC_000004.10:g.106358825_106358827del NCBI36
NG_028191.1:g.77345_77347del , LRG_626:g.77345_77347del

Transcript Alleles

HGVS Amino-acid change
ENST00000380013.9:c.-46-15678_-46-15676del (TET2) MANE Select ENSP00000369351.4:n.-46-15678_-46-15676de...
ENST00000265149.9:c.-46-15678_-46-15676del (TET2) ENSP00000265149.5:n.-46-15678_-46-15676de...
ENST00000305737.6:c.-46-15678_-46-15676del (TET2) ENSP00000306705.2:n.-46-15678_-46-15676de...
ENST00000380013.8:c.-46-15678_-46-15676del (TET2) ENSP00000369351.4:n.-46-15678_-46-15676de...
ENST00000394764.2:c.-46-15678_-46-15676del (TET2) ENSP00000378245.2:n.-46-15678_-46-15676de...
ENST00000413648.2:c.-46-15678_-46-15676del (TET2) ENSP00000391448.2:n.-46-15678_-46-15676de...
ENST00000513237.5:c.18-15678_18-15676del (TET2) ENSP00000425443.1:n.18-15678_18-15676del
ENST00000514870.1:c.-46-15678_-46-15676del (TET2) ENSP00000426885.1:n.-46-15678_-46-15676de...
ENST00000540549.5:c.-46-15678_-46-15676del (TET2) ENSP00000442788.1:n.-46-15678_-46-15676de...
NM_001127208.2:c.-46-15678_-46-15676del , LRG_626t1:c.-46-15678_-46-15676del (TET2) NP_001120680.1:n.-46-15678_-46-15676del
NM_017628.4:c.-46-15678_-46-15676del , LRG_626t2:c.-46-15678_-46-15676del (TET2) NP_060098.3:n.-46-15678_-46-15676del
NR_126420.1:n.319-40546_319-40544del (TET2-AS1)
XM_005263082.1:c.-46-15678_-46-15676del (TET2) XP_005263139.1:n.-46-15678_-46-15676del
XM_006714242.2:c.-46-15678_-46-15676del (TET2) XP_006714305.1:n.-46-15678_-46-15676del
XM_011532043.1:c.-46-15678_-46-15676del (TET2) XP_011530345.1:n.-46-15678_-46-15676del
XR_244633.2:n.251-15678_251-15676del (TET2)
XR_244634.2:n.251-15678_251-15676del (TET2)
XR_427546.2:n.251-15678_251-15676del (TET2)
XR_938746.1:n.251-15678_251-15676del (TET2)
XR_938747.1:n.251-15678_251-15676del (TET2)
XM_005263082.3:c.-46-15678_-46-15676del (TET2) XP_005263139.1:n.-46-15678_-46-15676del
XM_006714242.3:c.-46-15678_-46-15676del (TET2) XP_006714305.1:n.-46-15678_-46-15676del
XM_017008319.1:c.-46-15678_-46-15676del (TET2) XP_016863808.1:n.-46-15678_-46-15676del
XM_024454102.1:c.-46-15678_-46-15676del (TET2) XP_024309870.1:n.-46-15678_-46-15676del
XM_024454103.1:c.-46-15678_-46-15676del (TET2) XP_024309871.1:n.-46-15678_-46-15676del
XR_001741246.1:n.286-15678_286-15676del (TET2)
XR_244633.3:n.286-15678_286-15676del (TET2)
XR_427546.4:n.286-15678_286-15676del (TET2)
XR_938746.2:n.286-15678_286-15676del (TET2)
XR_938747.3:n.286-15678_286-15676del (TET2)
NM_001127208.3:c.-46-15678_-46-15676del (TET2) MANE Select NP_001120680.1:n.-46-15678_-46-15676del