Canonical Allele Identifier: CA357804718
Community Standard Title: NM_001127208.3(TET2):c.3594+1G>C
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105242928G>C , CM000666.2:g.105242928G>C GRCh38
NC_000004.11:g.106164085G>C , CM000666.1:g.106164085G>C GRCh37
NC_000004.10:g.106383534G>C NCBI36
NG_028191.1:g.102054G>C , LRG_626:g.102054G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001127208.3:c.3594+1G>C (TET2) MANE Select NP_001120680.1:n.3594+1G>C
ENST00000380013.9:c.3594+1G>C (TET2) MANE Select ENSP00000369351.4:n.3594+1G>C
NM_001127208.2:c.3594+1G>C , LRG_626t1:c.3594+1G>C (TET2) NP_001120680.1:n.3594+1G>C
NR_126420.1:n.319-65256C>G (TET2-AS1)
ENST00000265149.9:c.3503+1G>C (TET2) ENSP00000265149.5:n.3503+1G>C
ENST00000380013.8:c.3594+1G>C (TET2) ENSP00000369351.4:n.3594+1G>C
ENST00000513237.5:c.3657+1G>C (TET2) ENSP00000425443.1:n.3657+1G>C
ENST00000540549.5:c.3594+1G>C (TET2) ENSP00000442788.1:n.3594+1G>C
XM_005263082.1:c.3594+1G>C (TET2) XP_005263139.1:n.3594+1G>C
XM_005263082.3:c.3594+1G>C (TET2) XP_005263139.1:n.3594+1G>C
XM_006714242.2:c.3503+1G>C (TET2) XP_006714305.1:n.3503+1G>C
XM_006714242.3:c.3503+1G>C (TET2) XP_006714305.1:n.3503+1G>C
XM_011532044.1:c.105+1G>C (TET2) XP_011530346.1:n.105+1G>C
XM_024454102.1:c.3594+1G>C (TET2) XP_024309870.1:n.3594+1G>C
XM_024454103.1:c.3594+1G>C (TET2) XP_024309871.1:n.3594+1G>C
XR_001741246.1:n.3964+1G>C (TET2)
XR_244633.2:n.3705+5577G>C (TET2)
XR_244633.3:n.3740+5577G>C (TET2)
XR_244634.2:n.3799+1G>C (TET2)
XR_427546.2:n.3890+1G>C (TET2)
XR_427546.4:n.3925+1G>C (TET2)
XR_938746.2:n.4126G>C (TET2)