Canonical Allele Identifier: CA1482655733

Gene: TET2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105163566_105163567delinsTC , CM000666.2:g.105163566_105163567delinsTC	GRCh38
NC_000004.11:g.106084723_106084724delinsTC , CM000666.1:g.106084723_106084724delinsTC	GRCh37
NC_000004.10:g.106304172_106304173delinsTC	NCBI36
NG_028191.1:g.22692_22693delinsTC , LRG_626:g.22692_22693delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380013.9:c.-193+16587_-193+16588delinsTC MANE Select	ENSP00000369351.4:n.-193+16587_-193+16588delinsTC
ENST00000265149.9:c.-193+16587_-193+16588delinsTC	ENSP00000265149.5:n.-193+16587_-193+16588delinsTC
ENST00000305737.6:c.-193+17480_-193+17481delinsTC	ENSP00000306705.2:n.-193+17480_-193+17481delinsTC
ENST00000380013.8:c.-193+16587_-193+16588delinsTC	ENSP00000369351.4:n.-193+16587_-193+16588delinsTC
ENST00000394764.2:c.-47+16587_-47+16588delinsTC	ENSP00000378245.2:n.-47+16587_-47+16588delinsTC
ENST00000413648.2:c.-47+16587_-47+16588delinsTC	ENSP00000391448.2:n.-47+16587_-47+16588delinsTC
ENST00000504042.5:n.102+16587_102+16588delinsTC
ENST00000505801.1:n.47+16587_47+16588delinsTC
ENST00000513237.5:c.-111+16587_-111+16588delinsTC	ENSP00000425443.1:n.-111+16587_-111+16588delinsTC
ENST00000514870.1:c.-193+15767_-193+15768delinsTC	ENSP00000426885.1:n.-193+15767_-193+15768delinsTC
ENST00000540549.5:c.-174+16587_-174+16588delinsTC	ENSP00000442788.1:n.-174+16587_-174+16588delinsTC
NM_001127208.2:c.-193+16587_-193+16588delinsTC , LRG_626t1:c.-193+16587_-193+16588delinsTC	NP_001120680.1:n.-193+16587_-193+16588delinsTC
NM_017628.4:c.-193+17480_-193+17481delinsTC , LRG_626t2:c.-193+17480_-193+17481delinsTC	NP_060098.3:n.-193+17480_-193+17481delinsTC
XM_005263082.1:c.-47+16587_-47+16588delinsTC	XP_005263139.1:n.-47+16587_-47+16588delinsTC
XM_006714242.2:c.-193+16587_-193+16588delinsTC	XP_006714305.1:n.-193+16587_-193+16588delinsTC
XM_011532043.1:c.-193+16587_-193+16588delinsTC	XP_011530345.1:n.-193+16587_-193+16588delinsTC
XR_244633.2:n.104+16587_104+16588delinsTC
XR_244634.2:n.104+16587_104+16588delinsTC
XR_427546.2:n.104+16587_104+16588delinsTC
XR_938746.1:n.104+16587_104+16588delinsTC
XR_938747.1:n.104+16587_104+16588delinsTC
XM_005263082.3:c.-47+16587_-47+16588delinsTC	XP_005263139.1:n.-47+16587_-47+16588delinsTC
XM_006714242.3:c.-193+16587_-193+16588delinsTC	XP_006714305.1:n.-193+16587_-193+16588delinsTC
XM_017008319.1:c.-193+16587_-193+16588delinsTC	XP_016863808.1:n.-193+16587_-193+16588delinsTC
XM_024454102.1:c.-305-8249_-305-8248delinsTC	XP_024309870.1:n.-305-8249_-305-8248delinsTC
XM_024454103.1:c.-193+17480_-193+17481delinsTC	XP_024309871.1:n.-193+17480_-193+17481delinsTC
XR_001741246.1:n.139+16587_139+16588delinsTC
XR_244633.3:n.139+16587_139+16588delinsTC
XR_427546.4:n.139+16587_139+16588delinsTC
XR_938746.2:n.139+16587_139+16588delinsTC
XR_938747.3:n.139+16587_139+16588delinsTC
NM_001127208.3:c.-193+16587_-193+16588delinsTC MANE Select	NP_001120680.1:n.-193+16587_-193+16588delinsTC