Canonical Allele Identifier: CA1239262683

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1674427984

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244160_25244161del , CM000664.2:g.25244160_25244161del	GRCh38
NC_000002.11:g.25467029_25467030del , CM000664.1:g.25467029_25467030del	GRCh37
NC_000002.10:g.25320533_25320534del	NCBI36
NG_029465.2:g.103430_103431del , LRG_459:g.103430_103431del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.164_165del
ENST00000683393.1:c.991_992del	ENSP00000508654.1:n.991_992del
ENST00000683760.1:c.1176_1177del	ENSP00000507765.1:p.Glu393IlefsTer2
ENST00000321117.10:c.1845_1846del MANE Select	ENSP00000324375.5:p.Glu616IlefsTer2
ENST00000264709.7:c.1845_1846del	ENSP00000264709.3:p.Glu616IlefsTer2
ENST00000321117.9:c.1845_1846del	ENSP00000324375.5:p.Glu616IlefsTer2
ENST00000380746.8:c.1278_1279del	ENSP00000370122.4:p.Glu427IlefsTer2
ENST00000380756.7:c.1845_1846del	ENSP00000370132.3:p.Glu616IlefsTer2
ENST00000402667.1:c.1176_1177del	ENSP00000384237.1:p.Glu393IlefsTer2
ENST00000474887.5:n.164_165del
NM_022552.4:c.1845_1846del , LRG_459t1:c.1845_1846del	NP_072046.2:p.Glu616IlefsTer2
NM_153759.3:c.1278_1279del , LRG_459t2:c.1278_1279del	NP_715640.2:p.Glu427IlefsTer2
NM_175629.2:c.1845_1846del , LRG_459t4:c.1845_1846del	NP_783328.1:p.Glu616IlefsTer2
XM_005264175.3:c.1845_1846del	XP_005264232.1:p.Glu616IlefsTer2
XM_005264177.3:c.1176_1177del	XP_005264234.1:p.Glu393IlefsTer2
XM_006711957.2:c.1845_1846del	XP_006712020.1:p.Glu616IlefsTer2
XM_006711958.2:c.1401_1402del	XP_006712021.1:p.Glu468IlefsTer2
XM_011532662.1:c.1698_1699del	XP_011530964.1:p.Glu567IlefsTer2
XM_011532663.1:c.1680_1681del	XP_011530965.1:p.Glu561IlefsTer2
XM_011532664.1:c.1845_1846del	XP_011530966.1:p.Glu616IlefsTer2
XM_011532665.1:c.1389_1390del	XP_011530967.1:p.Glu464IlefsTer2
XM_011532666.1:c.1317_1318del	XP_011530968.1:p.Glu440IlefsTer2
XM_011532667.1:c.1176_1177del	XP_011530969.1:p.Glu393IlefsTer2
XM_011532668.1:c.1845_1846del	XP_011530970.1:p.Glu616IlefsTer2
NM_001320893.1:c.1389_1390del	NP_001307822.1:p.Glu464IlefsTer2
NR_135490.1:n.2183_2184del
XM_005264175.5:c.1845_1846del	XP_005264232.1:p.Glu616IlefsTer2
XM_005264177.4:c.1176_1177del	XP_005264234.1:p.Glu393IlefsTer2
XM_011532662.2:c.1698_1699del	XP_011530964.1:p.Glu567IlefsTer2
XM_011532663.2:c.1680_1681del	XP_011530965.1:p.Glu561IlefsTer2
XM_011532664.2:c.1845_1846del	XP_011530966.1:p.Glu616IlefsTer2
XM_011532666.2:c.1317_1318del	XP_011530968.1:p.Glu440IlefsTer2
XM_011532667.3:c.1176_1177del	XP_011530969.1:p.Glu393IlefsTer2
XM_017003526.1:c.1845_1846del	XP_016859015.1:p.Glu616IlefsTer2
XM_017003527.1:c.1176_1177del	XP_016859016.1:p.Glu393IlefsTer2
XR_001738657.1:n.2122_2123del
NM_001375819.1:c.1176_1177del	NP_001362748.1:p.Glu393IlefsTer2
NR_135490.2:n.2076_2077del
NM_022552.5:c.1845_1846del MANE Select	NP_072046.2:p.Glu616IlefsTer2