Canonical Allele Identifier: CA3032126

Gene: TET2 TET2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105243757G>A , CM000666.2:g.105243757G>A	GRCh38
NC_000004.11:g.106164914G>A , CM000666.1:g.106164914G>A	GRCh37
NC_000004.10:g.106384363G>A	NCBI36
NG_028191.1:g.102883G>A , LRG_626:g.102883G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001127208.3:c.3782G>A (TET2) MANE Select	NP_001120680.1:p.Arg1261His
ENST00000380013.9:c.3782G>A (TET2) MANE Select	ENSP00000369351.4:p.Arg1261His
NM_001127208.2:c.3782G>A , LRG_626t1:c.3782G>A (TET2)	NP_001120680.1:p.Arg1261His
NR_126420.1:n.319-66085C>T (TET2-AS1)
ENST00000265149.9:c.*106G>A (TET2)	ENSP00000265149.5:n.*106G>A
ENST00000380013.8:c.3782G>A (TET2)	ENSP00000369351.4:p.Arg1261His
ENST00000513237.5:c.3845G>A (TET2)	ENSP00000425443.1:p.Arg1282His
ENST00000540549.5:c.3782G>A (TET2)	ENSP00000442788.1:p.Arg1261His
XM_005263082.1:c.3782G>A (TET2)	XP_005263139.1:p.Arg1261His
XM_005263082.3:c.3782G>A (TET2)	XP_005263139.1:p.Arg1261His
XM_006714242.2:c.3503+830G>A (TET2)	XP_006714305.1:n.3503+830G>A
XM_006714242.3:c.3503+830G>A (TET2)	XP_006714305.1:n.3503+830G>A
XM_011532044.1:c.293G>A (TET2)	XP_011530346.1:p.Arg98His
XM_024454102.1:c.3782G>A (TET2)	XP_024309870.1:p.Arg1261His
XM_024454103.1:c.3782G>A (TET2)	XP_024309871.1:p.Arg1261His
XR_001741246.1:n.3964+830G>A (TET2)
XR_244633.2:n.3705+6406G>A (TET2)
XR_244633.3:n.3740+6406G>A (TET2)
XR_244634.2:n.3987G>A (TET2)
XR_427546.2:n.3890+830G>A (TET2)
XR_427546.4:n.3925+830G>A (TET2)