Canonical Allele Identifier: CA50437642
Gene: TET3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74018650T>C , CM000664.2:g.74018650T>C GRCh38
NC_000002.11:g.74245777T>C , CM000664.1:g.74245777T>C GRCh37
NC_000002.10:g.74099285T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000409262.8:c.360+15484T>C MANE Select ENSP00000386869.3:n.360+15484T>C
ENST00000305799.8:c.81+15484T>C ENSP00000307803.8:n.81+15484T>C
ENST00000409262.7:c.360+15484T>C ENSP00000386869.3:n.360+15484T>C
NM_001287491.1:c.360+15484T>C NP_001274420.1:n.360+15484T>C
XM_005264187.2:c.360+15484T>C XP_005264244.1:n.360+15484T>C
XM_011532682.1:c.360+15484T>C XP_011530984.1:n.360+15484T>C
XM_011532683.1:c.360+15484T>C XP_011530985.1:n.360+15484T>C
XM_011532684.1:c.360+15484T>C XP_011530986.1:n.360+15484T>C
XM_011532685.1:c.304-27628T>C XP_011530987.1:n.304-27628T>C
XM_011532686.1:c.304-27628T>C XP_011530988.1:n.304-27628T>C
XM_011532687.1:c.81+15484T>C XP_011530989.1:n.81+15484T>C
XM_011532688.1:c.360+15484T>C XP_011530990.1:n.360+15484T>C
XM_011532689.1:c.-81+15484T>C XP_011530991.1:n.-81+15484T>C
XM_011532690.1:c.-81+31944T>C XP_011530992.1:n.-81+31944T>C
NM_001287491.2:c.360+15484T>C MANE Select NP_001274420.1:n.360+15484T>C
NM_001366022.1:c.81+15484T>C NP_001352951.1:n.81+15484T>C
XM_011532682.2:c.360+15484T>C XP_011530984.1:n.360+15484T>C
XM_011532683.2:c.360+15484T>C XP_011530985.1:n.360+15484T>C
XM_011532684.2:c.360+15484T>C XP_011530986.1:n.360+15484T>C
XM_011532685.2:c.304-27628T>C XP_011530987.1:n.304-27628T>C
XM_011532686.2:c.304-27628T>C XP_011530988.1:n.304-27628T>C
XM_011532687.2:c.81+15484T>C XP_011530989.1:n.81+15484T>C
XM_011532688.2:c.360+15484T>C XP_011530990.1:n.360+15484T>C
XM_017003566.1:c.360+15484T>C XP_016859055.1:n.360+15484T>C
XM_024452745.1:c.360+15484T>C XP_024308513.1:n.360+15484T>C
XM_024452746.1:c.360+15484T>C XP_024308514.1:n.360+15484T>C
XM_024452747.1:c.-81+15484T>C XP_024308515.1:n.-81+15484T>C
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