Canonical Allele Identifier: CA357805331
Community Standard Title: NM_001127208.3(TET2):c.3765C>A (p.Tyr1255Ter)
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105243740C>A , CM000666.2:g.105243740C>A GRCh38
NC_000004.11:g.106164897C>A , CM000666.1:g.106164897C>A GRCh37
NC_000004.10:g.106384346C>A NCBI36
NG_028191.1:g.102866C>A , LRG_626:g.102866C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001127208.3:c.3765C>A (TET2) MANE Select NP_001120680.1:p.Tyr1255Ter
ENST00000380013.9:c.3765C>A (TET2) MANE Select ENSP00000369351.4:p.Tyr1255Ter
NM_001127208.2:c.3765C>A , LRG_626t1:c.3765C>A (TET2) NP_001120680.1:p.Tyr1255Ter
NR_126420.1:n.319-66068G>T (TET2-AS1)
ENST00000265149.9:c.*89C>A (TET2) ENSP00000265149.5:n.*89C>A
ENST00000380013.8:c.3765C>A (TET2) ENSP00000369351.4:p.Tyr1255Ter
ENST00000513237.5:c.3828C>A (TET2) ENSP00000425443.1:p.Tyr1276Ter
ENST00000540549.5:c.3765C>A (TET2) ENSP00000442788.1:p.Tyr1255Ter
XM_005263082.1:c.3765C>A (TET2) XP_005263139.1:p.Tyr1255Ter
XM_005263082.3:c.3765C>A (TET2) XP_005263139.1:p.Tyr1255Ter
XM_006714242.2:c.3503+813C>A (TET2) XP_006714305.1:n.3503+813C>A
XM_006714242.3:c.3503+813C>A (TET2) XP_006714305.1:n.3503+813C>A
XM_011532044.1:c.276C>A (TET2) XP_011530346.1:p.Tyr92Ter
XM_024454102.1:c.3765C>A (TET2) XP_024309870.1:p.Tyr1255Ter
XM_024454103.1:c.3765C>A (TET2) XP_024309871.1:p.Tyr1255Ter
XR_001741246.1:n.3964+813C>A (TET2)
XR_244633.2:n.3705+6389C>A (TET2)
XR_244633.3:n.3740+6389C>A (TET2)
XR_244634.2:n.3970C>A (TET2)
XR_427546.2:n.3890+813C>A (TET2)
XR_427546.4:n.3925+813C>A (TET2)