Canonical Allele Identifier: CA553594622

Gene: TET2 TET2-AS1

Linked Data

• dbSNP Id: rs1403843487
• gnomAD v2: 4-106199319-AAATATATACATATATATATATATATATATATATATAT-A
• gnomAD v3: 4-105278162-AAATATATACATATATATATATATATATATATATATAT-A
• gnomAD v4: 4-105278162-AAATATATACATATATATATATATATATATATATATAT-A
• MyVariant Identifiers: chr4:g.106199320_106199356del (hg19) ; chr4:g.105278163_105278199del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105278164_105278200del , CM000666.2:g.105278164_105278200del	GRCh38
NC_000004.11:g.106199321_106199357del , CM000666.1:g.106199321_106199357del	GRCh37
NC_000004.10:g.106418770_106418806del	NCBI36
NG_028191.1:g.137290_137326del , LRG_626:g.137290_137326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380013.9:c.*1645_*1681del (TET2) MANE Select	ENSP00000369351.4:n.*1645_*1681del
ENST00000265149.9:c.*3978_*4014del (TET2)	ENSP00000265149.5:n.*3978_*4014del
ENST00000380013.8:c.*1645_*1681del (TET2)	ENSP00000369351.4:n.*1645_*1681del
ENST00000513237.5:c.*1645_*1681del (TET2)	ENSP00000425443.1:n.*1645_*1681del
ENST00000540549.5:c.*1645_*1681del (TET2)	ENSP00000442788.1:n.*1645_*1681del
NM_001127208.2:c.*1645_*1681del , LRG_626t1:c.*1645_*1681del (TET2)	NP_001120680.1:n.*1645_*1681del
NR_126420.1:n.318+56187_318+56223del (TET2-AS1)
XM_005263082.1:c.*1645_*1681del (TET2)	XP_005263139.1:n.*1645_*1681del
XM_006714242.2:c.*1645_*1681del (TET2)	XP_006714305.1:n.*1645_*1681del
XM_011532044.1:c.*1645_*1681del (TET2)	XP_011530346.1:n.*1645_*1681del
XR_244633.2:n.7556_7592del (TET2)
XR_244634.2:n.7859_7895del (TET2)
XM_005263082.3:c.*1645_*1681del (TET2)	XP_005263139.1:n.*1645_*1681del
XM_006714242.3:c.*1645_*1681del (TET2)	XP_006714305.1:n.*1645_*1681del
XM_024454102.1:c.*1645_*1681del (TET2)	XP_024309870.1:n.*1645_*1681del
XM_024454103.1:c.*1645_*1681del (TET2)	XP_024309871.1:n.*1645_*1681del
XR_244633.3:n.7591_7627del (TET2)
NM_001127208.3:c.*1645_*1681del (TET2) MANE Select	NP_001120680.1:n.*1645_*1681del