Canonical Allele Identifier: CA347315159

Gene: TET3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74099456C>T , CM000664.2:g.74099456C>T	GRCh38
NC_000002.11:g.74326583C>T , CM000664.1:g.74326583C>T	GRCh37
NC_000002.10:g.74180091C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409262.8:c.3448C>T MANE Select	ENSP00000386869.3:p.Arg1150Ter
ENST00000305799.8:c.3169C>T	ENSP00000307803.8:p.Arg1057Ter
ENST00000409262.7:c.3448C>T	ENSP00000386869.3:p.Arg1150Ter
NM_001287491.1:c.3448C>T	NP_001274420.1:p.Arg1150Ter
XM_005264187.2:c.3448C>T	XP_005264244.1:p.Arg1150Ter
XM_011532682.1:c.3496C>T	XP_011530984.1:p.Arg1166Ter
XM_011532683.1:c.3496C>T	XP_011530985.1:p.Arg1166Ter
XM_011532684.1:c.3496C>T	XP_011530986.1:p.Arg1166Ter
XM_011532685.1:c.3439C>T	XP_011530987.1:p.Arg1147Ter
XM_011532686.1:c.3391C>T	XP_011530988.1:p.Arg1131Ter
XM_011532687.1:c.3217C>T	XP_011530989.1:p.Arg1073Ter
XM_011532689.1:c.922C>T	XP_011530991.1:p.Arg308Ter
XM_011532690.1:c.922C>T	XP_011530992.1:p.Arg308Ter
NM_001287491.2:c.3448C>T MANE Select	NP_001274420.1:p.Arg1150Ter
NM_001366022.1:c.3169C>T	NP_001352951.1:p.Arg1057Ter
XM_011532682.2:c.3496C>T	XP_011530984.1:p.Arg1166Ter
XM_011532683.2:c.3496C>T	XP_011530985.1:p.Arg1166Ter
XM_011532684.2:c.3496C>T	XP_011530986.1:p.Arg1166Ter
XM_011532685.2:c.3439C>T	XP_011530987.1:p.Arg1147Ter
XM_011532686.2:c.3391C>T	XP_011530988.1:p.Arg1131Ter
XM_011532687.2:c.3217C>T	XP_011530989.1:p.Arg1073Ter
XM_017003566.1:c.3496C>T	XP_016859055.1:p.Arg1166Ter
XM_024452745.1:c.3315+5790C>T	XP_024308513.1:n.3315+5790C>T
XM_024452746.1:c.3267+5790C>T	XP_024308514.1:n.3267+5790C>T
XM_024452747.1:c.922C>T	XP_024308515.1:p.Arg308Ter