Canonical Allele Identifier: CA1066300399

Gene: TET2 TET2-AS1

Linked Data

• gnomAD v3: 4-105185181-TCCTTCA-T
• gnomAD v4: 4-105185181-TCCTTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105185182_105185187del , CM000666.2:g.105185182_105185187del	GRCh38
NC_000004.11:g.106106339_106106344del , CM000666.1:g.106106339_106106344del	GRCh37
NC_000004.10:g.106325788_106325793del	NCBI36
NG_028191.1:g.44308_44313del , LRG_626:g.44308_44313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380013.9:c.-192-5178_-192-5173del (TET2) MANE Select	ENSP00000369351.4:n.-192-5178_-192-5173del
ENST00000265149.9:c.-192-5178_-192-5173del (TET2)	ENSP00000265149.5:n.-192-5178_-192-5173del
ENST00000305737.6:c.-192-5178_-192-5173del (TET2)	ENSP00000306705.2:n.-192-5178_-192-5173del
ENST00000380013.8:c.-192-5178_-192-5173del (TET2)	ENSP00000369351.4:n.-192-5178_-192-5173del
ENST00000394764.2:c.-47+38203_-47+38208del (TET2)	ENSP00000378245.2:n.-47+38203_-47+38208del
ENST00000413648.2:c.-47+38203_-47+38208del (TET2)	ENSP00000391448.2:n.-47+38203_-47+38208del
ENST00000504042.5:n.103-5178_103-5173del (TET2)
ENST00000505801.1:n.48-5178_48-5173del (TET2)
ENST00000513237.5:c.-110-5178_-110-5173del (TET2)	ENSP00000425443.1:n.-110-5178_-110-5173del
ENST00000514870.1:c.-192-5178_-192-5173del (TET2)	ENSP00000426885.1:n.-192-5178_-192-5173del
ENST00000540549.5:c.-173-5178_-173-5173del (TET2)	ENSP00000442788.1:n.-173-5178_-173-5173del
NM_001127208.2:c.-192-5178_-192-5173del , LRG_626t1:c.-192-5178_-192-5173del (TET2)	NP_001120680.1:n.-192-5178_-192-5173del
NM_017628.4:c.-192-5178_-192-5173del , LRG_626t2:c.-192-5178_-192-5173del (TET2)	NP_060098.3:n.-192-5178_-192-5173del
NR_126420.1:n.319-7515_319-7510del (TET2-AS1)
XM_005263082.1:c.-47+38203_-47+38208del (TET2)	XP_005263139.1:n.-47+38203_-47+38208del
XM_006714242.2:c.-192-5178_-192-5173del (TET2)	XP_006714305.1:n.-192-5178_-192-5173del
XM_011532043.1:c.-192-5178_-192-5173del (TET2)	XP_011530345.1:n.-192-5178_-192-5173del
XR_244633.2:n.105-5178_105-5173del (TET2)
XR_244634.2:n.105-5178_105-5173del (TET2)
XR_427546.2:n.105-5178_105-5173del (TET2)
XR_938746.1:n.105-5178_105-5173del (TET2)
XR_938747.1:n.105-5178_105-5173del (TET2)
XM_005263082.3:c.-47+38203_-47+38208del (TET2)	XP_005263139.1:n.-47+38203_-47+38208del
XM_006714242.3:c.-192-5178_-192-5173del (TET2)	XP_006714305.1:n.-192-5178_-192-5173del
XM_017008319.1:c.-192-5178_-192-5173del (TET2)	XP_016863808.1:n.-192-5178_-192-5173del
XM_024454102.1:c.-192-5178_-192-5173del (TET2)	XP_024309870.1:n.-192-5178_-192-5173del
XM_024454103.1:c.-192-5178_-192-5173del (TET2)	XP_024309871.1:n.-192-5178_-192-5173del
XR_001741246.1:n.140-5178_140-5173del (TET2)
XR_244633.3:n.140-5178_140-5173del (TET2)
XR_427546.4:n.140-5178_140-5173del (TET2)
XR_938746.2:n.140-5178_140-5173del (TET2)
XR_938747.3:n.140-5178_140-5173del (TET2)
NM_001127208.3:c.-192-5178_-192-5173del (TET2) MANE Select	NP_001120680.1:n.-192-5178_-192-5173del