Canonical Allele Identifier: CA2658168546

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244229-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244229_25244230insTT , CM000664.2:g.25244229_25244230insTT	GRCh38
NC_000002.11:g.25467098_25467099insTT , CM000664.1:g.25467098_25467099insTT	GRCh37
NC_000002.10:g.25320602_25320603insTT	NCBI36
NG_029465.2:g.103361_103362insAA , LRG_459:g.103361_103362insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.95_96insAA
ENST00000683393.1:c.922_923insAA	ENSP00000508654.1:n.922_923insAA
ENST00000683760.1:c.1107_1108insAA	ENSP00000507765.1:p.Gly370LysfsTer?
ENST00000321117.10:c.1776_1777insAA MANE Select	ENSP00000324375.5:p.Gly593LysfsTer?
ENST00000264709.7:c.1776_1777insAA	ENSP00000264709.3:p.Gly593LysfsTer?
ENST00000321117.9:c.1776_1777insAA	ENSP00000324375.5:p.Gly593LysfsTer?
ENST00000380746.8:c.1209_1210insAA	ENSP00000370122.4:p.Gly404LysfsTer?
ENST00000380756.7:c.1776_1777insAA	ENSP00000370132.3:p.Gly593LysfsTer?
ENST00000402667.1:c.1107_1108insAA	ENSP00000384237.1:p.Gly370LysfsTer?
ENST00000474887.5:n.95_96insAA
NM_022552.4:c.1776_1777insAA , LRG_459t1:c.1776_1777insAA	NP_072046.2:p.Gly593LysfsTer?
NM_153759.3:c.1209_1210insAA , LRG_459t2:c.1209_1210insAA	NP_715640.2:p.Gly404LysfsTer?
NM_175629.2:c.1776_1777insAA , LRG_459t4:c.1776_1777insAA	NP_783328.1:p.Gly593LysfsTer?
XM_005264175.3:c.1776_1777insAA	XP_005264232.1:p.Gly593LysfsTer?
XM_005264177.3:c.1107_1108insAA	XP_005264234.1:p.Gly370LysfsTer?
XM_006711957.2:c.1776_1777insAA	XP_006712020.1:p.Gly593LysfsTer?
XM_006711958.2:c.1332_1333insAA	XP_006712021.1:p.Gly445LysfsTer?
XM_011532662.1:c.1629_1630insAA	XP_011530964.1:p.Gly544LysfsTer?
XM_011532663.1:c.1611_1612insAA	XP_011530965.1:p.Gly538LysfsTer?
XM_011532664.1:c.1776_1777insAA	XP_011530966.1:p.Gly593LysfsTer?
XM_011532665.1:c.1320_1321insAA	XP_011530967.1:p.Gly441LysfsTer?
XM_011532666.1:c.1248_1249insAA	XP_011530968.1:p.Gly417LysfsTer?
XM_011532667.1:c.1107_1108insAA	XP_011530969.1:p.Gly370LysfsTer?
XM_011532668.1:c.1776_1777insAA	XP_011530970.1:p.Gly593LysfsTer?
NM_001320893.1:c.1320_1321insAA	NP_001307822.1:p.Gly441LysfsTer?
NR_135490.1:n.2114_2115insAA
XM_005264175.5:c.1776_1777insAA	XP_005264232.1:p.Gly593LysfsTer?
XM_005264177.4:c.1107_1108insAA	XP_005264234.1:p.Gly370LysfsTer?
XM_011532662.2:c.1629_1630insAA	XP_011530964.1:p.Gly544LysfsTer?
XM_011532663.2:c.1611_1612insAA	XP_011530965.1:p.Gly538LysfsTer?
XM_011532664.2:c.1776_1777insAA	XP_011530966.1:p.Gly593LysfsTer?
XM_011532666.2:c.1248_1249insAA	XP_011530968.1:p.Gly417LysfsTer?
XM_011532667.3:c.1107_1108insAA	XP_011530969.1:p.Gly370LysfsTer?
XM_017003526.1:c.1776_1777insAA	XP_016859015.1:p.Gly593LysfsTer?
XM_017003527.1:c.1107_1108insAA	XP_016859016.1:p.Gly370LysfsTer?
XR_001738657.1:n.2053_2054insAA
NM_001375819.1:c.1107_1108insAA	NP_001362748.1:p.Gly370LysfsTer?
NR_135490.2:n.2007_2008insAA
NM_022552.5:c.1776_1777insAA MANE Select	NP_072046.2:p.Gly593LysfsTer?