Canonical Allele Identifier: CA102734993

Gene: TET2 TET2-AS1

Linked Data

• dbSNP Id: rs950642475
• gnomAD v2: 4-106139885-GTA-G
• gnomAD v3: 4-105218728-GTA-G
• gnomAD v4: 4-105218728-GTA-G
• MyVariant Identifiers: chr4:g.106139886_106139887del (hg19) ; chr4:g.105218729_105218730del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105218732_105218733del , CM000666.2:g.105218732_105218733del	GRCh38
NC_000004.11:g.106139889_106139890del , CM000666.1:g.106139889_106139890del	GRCh37
NC_000004.10:g.106359338_106359339del	NCBI36
NG_028191.1:g.77858_77859del , LRG_626:g.77858_77859del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380013.9:c.-46-15165_-46-15164del (TET2) MANE Select	ENSP00000369351.4:n.-46-15165_-46-15164del
ENST00000265149.9:c.-46-15165_-46-15164del (TET2)	ENSP00000265149.5:n.-46-15165_-46-15164del
ENST00000305737.6:c.-46-15165_-46-15164del (TET2)	ENSP00000306705.2:n.-46-15165_-46-15164del
ENST00000380013.8:c.-46-15165_-46-15164del (TET2)	ENSP00000369351.4:n.-46-15165_-46-15164del
ENST00000394764.2:c.-46-15165_-46-15164del (TET2)	ENSP00000378245.2:n.-46-15165_-46-15164del
ENST00000413648.2:c.-46-15165_-46-15164del (TET2)	ENSP00000391448.2:n.-46-15165_-46-15164del
ENST00000513237.5:c.18-15165_18-15164del (TET2)	ENSP00000425443.1:n.18-15165_18-15164del
ENST00000514870.1:c.-46-15165_-46-15164del (TET2)	ENSP00000426885.1:n.-46-15165_-46-15164del
ENST00000540549.5:c.-46-15165_-46-15164del (TET2)	ENSP00000442788.1:n.-46-15165_-46-15164del
NM_001127208.2:c.-46-15165_-46-15164del , LRG_626t1:c.-46-15165_-46-15164del (TET2)	NP_001120680.1:n.-46-15165_-46-15164del
NM_017628.4:c.-46-15165_-46-15164del , LRG_626t2:c.-46-15165_-46-15164del (TET2)	NP_060098.3:n.-46-15165_-46-15164del
NR_126420.1:n.319-41058_319-41057del (TET2-AS1)
XM_005263082.1:c.-46-15165_-46-15164del (TET2)	XP_005263139.1:n.-46-15165_-46-15164del
XM_006714242.2:c.-46-15165_-46-15164del (TET2)	XP_006714305.1:n.-46-15165_-46-15164del
XM_011532043.1:c.-46-15165_-46-15164del (TET2)	XP_011530345.1:n.-46-15165_-46-15164del
XR_244633.2:n.251-15165_251-15164del (TET2)
XR_244634.2:n.251-15165_251-15164del (TET2)
XR_427546.2:n.251-15165_251-15164del (TET2)
XR_938746.1:n.251-15165_251-15164del (TET2)
XR_938747.1:n.251-15165_251-15164del (TET2)
XM_005263082.3:c.-46-15165_-46-15164del (TET2)	XP_005263139.1:n.-46-15165_-46-15164del
XM_006714242.3:c.-46-15165_-46-15164del (TET2)	XP_006714305.1:n.-46-15165_-46-15164del
XM_017008319.1:c.-46-15165_-46-15164del (TET2)	XP_016863808.1:n.-46-15165_-46-15164del
XM_024454102.1:c.-46-15165_-46-15164del (TET2)	XP_024309870.1:n.-46-15165_-46-15164del
XM_024454103.1:c.-46-15165_-46-15164del (TET2)	XP_024309871.1:n.-46-15165_-46-15164del
XR_001741246.1:n.286-15165_286-15164del (TET2)
XR_244633.3:n.286-15165_286-15164del (TET2)
XR_427546.4:n.286-15165_286-15164del (TET2)
XR_938746.2:n.286-15165_286-15164del (TET2)
XR_938747.3:n.286-15165_286-15164del (TET2)
NM_001127208.3:c.-46-15165_-46-15164del (TET2) MANE Select	NP_001120680.1:n.-46-15165_-46-15164del