Canonical Allele Identifier: CA1239262820

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244221_25244222delinsCA , CM000664.2:g.25244221_25244222delinsCA	GRCh38
NC_000002.11:g.25467090_25467091delinsCA , CM000664.1:g.25467090_25467091delinsCA	GRCh37
NC_000002.10:g.25320594_25320595delinsCA	NCBI36
NG_029465.2:g.103369_103370delinsTG , LRG_459:g.103369_103370delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.103_104delinsTG
ENST00000683393.1:c.930_931delinsTG	ENSP00000508654.1:n.930_931delinsTG
ENST00000683760.1:c.1115_1116delinsTG	ENSP00000507765.1:p.Leu372=
ENST00000321117.10:c.1784_1785delinsTG MANE Select	ENSP00000324375.5:p.Leu595=
ENST00000264709.7:c.1784_1785delinsTG	ENSP00000264709.3:p.Leu595=
ENST00000321117.9:c.1784_1785delinsTG	ENSP00000324375.5:p.Leu595=
ENST00000380746.8:c.1217_1218delinsTG	ENSP00000370122.4:p.Leu406=
ENST00000380756.7:c.1784_1785delinsTG	ENSP00000370132.3:p.Leu595=
ENST00000402667.1:c.1115_1116delinsTG	ENSP00000384237.1:p.Leu372=
ENST00000474887.5:n.103_104delinsTG
NM_022552.4:c.1784_1785delinsTG , LRG_459t1:c.1784_1785delinsTG	NP_072046.2:p.Leu595=
NM_153759.3:c.1217_1218delinsTG , LRG_459t2:c.1217_1218delinsTG	NP_715640.2:p.Leu406=
NM_175629.2:c.1784_1785delinsTG , LRG_459t4:c.1784_1785delinsTG	NP_783328.1:p.Leu595=
XM_005264175.3:c.1784_1785delinsTG	XP_005264232.1:p.Leu595=
XM_005264177.3:c.1115_1116delinsTG	XP_005264234.1:p.Leu372=
XM_006711957.2:c.1784_1785delinsTG	XP_006712020.1:p.Leu595=
XM_006711958.2:c.1340_1341delinsTG	XP_006712021.1:p.Leu447=
XM_011532662.1:c.1637_1638delinsTG	XP_011530964.1:p.Leu546=
XM_011532663.1:c.1619_1620delinsTG	XP_011530965.1:p.Leu540=
XM_011532664.1:c.1784_1785delinsTG	XP_011530966.1:p.Leu595=
XM_011532665.1:c.1328_1329delinsTG	XP_011530967.1:p.Leu443=
XM_011532666.1:c.1256_1257delinsTG	XP_011530968.1:p.Leu419=
XM_011532667.1:c.1115_1116delinsTG	XP_011530969.1:p.Leu372=
XM_011532668.1:c.1784_1785delinsTG	XP_011530970.1:p.Leu595=
NM_001320893.1:c.1328_1329delinsTG	NP_001307822.1:p.Leu443=
NR_135490.1:n.2122_2123delinsTG
XM_005264175.5:c.1784_1785delinsTG	XP_005264232.1:p.Leu595=
XM_005264177.4:c.1115_1116delinsTG	XP_005264234.1:p.Leu372=
XM_011532662.2:c.1637_1638delinsTG	XP_011530964.1:p.Leu546=
XM_011532663.2:c.1619_1620delinsTG	XP_011530965.1:p.Leu540=
XM_011532664.2:c.1784_1785delinsTG	XP_011530966.1:p.Leu595=
XM_011532666.2:c.1256_1257delinsTG	XP_011530968.1:p.Leu419=
XM_011532667.3:c.1115_1116delinsTG	XP_011530969.1:p.Leu372=
XM_017003526.1:c.1784_1785delinsTG	XP_016859015.1:p.Leu595=
XM_017003527.1:c.1115_1116delinsTG	XP_016859016.1:p.Leu372=
XR_001738657.1:n.2061_2062delinsTG
NM_001375819.1:c.1115_1116delinsTG	NP_001362748.1:p.Leu372=
NR_135490.2:n.2015_2016delinsTG
NM_022552.5:c.1784_1785delinsTG MANE Select	NP_072046.2:p.Leu595=