Canonical Allele Identifier: CA2576694298

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244231_25244232insCT , CM000664.2:g.25244231_25244232insCT	GRCh38
NC_000002.11:g.25467100_25467101insCT , CM000664.1:g.25467100_25467101insCT	GRCh37
NC_000002.10:g.25320604_25320605insCT	NCBI36
NG_029465.2:g.103360_103361insGA , LRG_459:g.103360_103361insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.94_95insGA
ENST00000683393.1:c.921_922insGA	ENSP00000508654.1:n.921_922insGA
ENST00000683760.1:c.1106_1107insGA	ENSP00000507765.1:p.Tyr369Ter
ENST00000321117.10:c.1775_1776insGA MANE Select	ENSP00000324375.5:p.Tyr592Ter
ENST00000264709.7:c.1775_1776insGA	ENSP00000264709.3:p.Tyr592Ter
ENST00000321117.9:c.1775_1776insGA	ENSP00000324375.5:p.Tyr592Ter
ENST00000380746.8:c.1208_1209insGA	ENSP00000370122.4:p.Tyr403Ter
ENST00000380756.7:c.1775_1776insGA	ENSP00000370132.3:p.Tyr592Ter
ENST00000402667.1:c.1106_1107insGA	ENSP00000384237.1:p.Tyr369Ter
ENST00000474887.5:n.94_95insGA
NM_022552.4:c.1775_1776insGA , LRG_459t1:c.1775_1776insGA	NP_072046.2:p.Tyr592Ter
NM_153759.3:c.1208_1209insGA , LRG_459t2:c.1208_1209insGA	NP_715640.2:p.Tyr403Ter
NM_175629.2:c.1775_1776insGA , LRG_459t4:c.1775_1776insGA	NP_783328.1:p.Tyr592Ter
XM_005264175.3:c.1775_1776insGA	XP_005264232.1:p.Tyr592Ter
XM_005264177.3:c.1106_1107insGA	XP_005264234.1:p.Tyr369Ter
XM_006711957.2:c.1775_1776insGA	XP_006712020.1:p.Tyr592Ter
XM_006711958.2:c.1331_1332insGA	XP_006712021.1:p.Tyr444Ter
XM_011532662.1:c.1628_1629insGA	XP_011530964.1:p.Tyr543Ter
XM_011532663.1:c.1610_1611insGA	XP_011530965.1:p.Tyr537Ter
XM_011532664.1:c.1775_1776insGA	XP_011530966.1:p.Tyr592Ter
XM_011532665.1:c.1319_1320insGA	XP_011530967.1:p.Tyr440Ter
XM_011532666.1:c.1247_1248insGA	XP_011530968.1:p.Tyr416Ter
XM_011532667.1:c.1106_1107insGA	XP_011530969.1:p.Tyr369Ter
XM_011532668.1:c.1775_1776insGA	XP_011530970.1:p.Tyr592Ter
NM_001320893.1:c.1319_1320insGA	NP_001307822.1:p.Tyr440Ter
NR_135490.1:n.2113_2114insGA
XM_005264175.5:c.1775_1776insGA	XP_005264232.1:p.Tyr592Ter
XM_005264177.4:c.1106_1107insGA	XP_005264234.1:p.Tyr369Ter
XM_011532662.2:c.1628_1629insGA	XP_011530964.1:p.Tyr543Ter
XM_011532663.2:c.1610_1611insGA	XP_011530965.1:p.Tyr537Ter
XM_011532664.2:c.1775_1776insGA	XP_011530966.1:p.Tyr592Ter
XM_011532666.2:c.1247_1248insGA	XP_011530968.1:p.Tyr416Ter
XM_011532667.3:c.1106_1107insGA	XP_011530969.1:p.Tyr369Ter
XM_017003526.1:c.1775_1776insGA	XP_016859015.1:p.Tyr592Ter
XM_017003527.1:c.1106_1107insGA	XP_016859016.1:p.Tyr369Ter
XR_001738657.1:n.2052_2053insGA
NM_001375819.1:c.1106_1107insGA	NP_001362748.1:p.Tyr369Ter
NR_135490.2:n.2006_2007insGA
NM_022552.5:c.1775_1776insGA MANE Select	NP_072046.2:p.Tyr592Ter