Canonical Allele Identifier: CA2535009908

Gene: TET2 TET2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105218297_105218298insGGACATAAATAATATTTTGA , CM000666.2:g.105218297_105218298insGGACATAAATAATATTTTGA	GRCh38
NC_000004.11:g.106139454_106139455insGGACATAAATAATATTTTGA , CM000666.1:g.106139454_106139455insGGACATAAATAATATTTTGA	GRCh37
NC_000004.10:g.106358903_106358904insGGACATAAATAATATTTTGA	NCBI36
NG_028191.1:g.77423_77424insGGACATAAATAATATTTTGA , LRG_626:g.77423_77424insGGACATAAATAATATTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380013.9:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2) MANE Select	ENSP00000369351.4:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000265149.9:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000265149.5:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000305737.6:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000306705.2:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000380013.8:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000369351.4:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000394764.2:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000378245.2:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000413648.2:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000391448.2:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000513237.5:c.18-15600_18-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000425443.1:n.18-15600_18-15599insGGACATAAATAATATTTTGA
ENST00000514870.1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000426885.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
ENST00000540549.5:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	ENSP00000442788.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTG...
NM_001127208.2:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA , LRG_626t1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	NP_001120680.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
NM_017628.4:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA , LRG_626t2:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	NP_060098.3:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
NR_126420.1:n.319-40626_319-40625insTCAAAATATTATTTATGTCC (TET2-AS1)
XM_005263082.1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_005263139.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XM_006714242.2:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_006714305.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XM_011532043.1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_011530345.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XR_244633.2:n.251-15600_251-15599insGGACATAAATAATATTTTGA (TET2)
XR_244634.2:n.251-15600_251-15599insGGACATAAATAATATTTTGA (TET2)
XR_427546.2:n.251-15600_251-15599insGGACATAAATAATATTTTGA (TET2)
XR_938746.1:n.251-15600_251-15599insGGACATAAATAATATTTTGA (TET2)
XR_938747.1:n.251-15600_251-15599insGGACATAAATAATATTTTGA (TET2)
XM_005263082.3:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_005263139.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XM_006714242.3:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_006714305.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XM_017008319.1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_016863808.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XM_024454102.1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_024309870.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XM_024454103.1:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2)	XP_024309871.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA
XR_001741246.1:n.286-15600_286-15599insGGACATAAATAATATTTTGA (TET2)
XR_244633.3:n.286-15600_286-15599insGGACATAAATAATATTTTGA (TET2)
XR_427546.4:n.286-15600_286-15599insGGACATAAATAATATTTTGA (TET2)
XR_938746.2:n.286-15600_286-15599insGGACATAAATAATATTTTGA (TET2)
XR_938747.3:n.286-15600_286-15599insGGACATAAATAATATTTTGA (TET2)
NM_001127208.3:c.-46-15600_-46-15599insGGACATAAATAATATTTTGA (TET2) MANE Select	NP_001120680.1:n.-46-15600_-46-15599insGGACATAAATAATATTTTGA