Canonical Allele Identifier: CA3031947
Community Standard Title: NM_001127208.3(TET2):c.2746C>T (p.Gln916Ter)
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105236688C>T , CM000666.2:g.105236688C>T GRCh38
NC_000004.11:g.106157845C>T , CM000666.1:g.106157845C>T GRCh37
NC_000004.10:g.106377294C>T NCBI36
NG_028191.1:g.95814C>T , LRG_626:g.95814C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001127208.3:c.2746C>T (TET2) MANE Select NP_001120680.1:p.Gln916Ter
ENST00000380013.9:c.2746C>T (TET2) MANE Select ENSP00000369351.4:p.Gln916Ter
NM_001127208.2:c.2746C>T , LRG_626t1:c.2746C>T (TET2) NP_001120680.1:p.Gln916Ter
NM_017628.4:c.2746C>T , LRG_626t2:c.2746C>T (TET2) NP_060098.3:p.Gln916Ter
NR_126420.1:n.319-59016G>A (TET2-AS1)
ENST00000265149.9:c.2746C>T (TET2) ENSP00000265149.5:p.Gln916Ter
ENST00000305737.6:c.2746C>T (TET2) ENSP00000306705.2:p.Gln916Ter
ENST00000380013.8:c.2746C>T (TET2) ENSP00000369351.4:p.Gln916Ter
ENST00000394764.2:c.*831C>T (TET2) ENSP00000378245.2:n.*831C>T
ENST00000413648.2:c.2746C>T (TET2) ENSP00000391448.2:p.Gln916Ter
ENST00000513237.5:c.2809C>T (TET2) ENSP00000425443.1:p.Gln937Ter
ENST00000540549.5:c.2746C>T (TET2) ENSP00000442788.1:p.Gln916Ter
XM_005263082.1:c.2746C>T (TET2) XP_005263139.1:p.Gln916Ter
XM_005263082.3:c.2746C>T (TET2) XP_005263139.1:p.Gln916Ter
XM_006714242.2:c.2746C>T (TET2) XP_006714305.1:p.Gln916Ter
XM_006714242.3:c.2746C>T (TET2) XP_006714305.1:p.Gln916Ter
XM_011532043.1:c.2746C>T (TET2) XP_011530345.1:p.Gln916Ter
XM_017008319.1:c.2746C>T (TET2) XP_016863808.1:p.Gln916Ter
XM_024454102.1:c.2746C>T (TET2) XP_024309870.1:p.Gln916Ter
XM_024454103.1:c.2746C>T (TET2) XP_024309871.1:p.Gln916Ter
XR_001741246.1:n.3077C>T (TET2)
XR_244633.2:n.3042C>T (TET2)
XR_244633.3:n.3077C>T (TET2)
XR_244634.2:n.3042C>T (TET2)
XR_427546.2:n.3042C>T (TET2)
XR_427546.4:n.3077C>T (TET2)
XR_938746.1:n.3042C>T (TET2)
XR_938746.2:n.3077C>T (TET2)
XR_938747.1:n.3042C>T (TET2)
XR_938747.3:n.3077C>T (TET2)