Canonical Allele Identifier: CA1239254694

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234413_25234414delinsCA , CM000664.2:g.25234413_25234414delinsCA	GRCh38
NC_000002.11:g.25457282_25457283delinsCA , CM000664.1:g.25457282_25457283delinsCA	GRCh37
NC_000002.10:g.25310786_25310787delinsCA	NCBI36
NG_029465.2:g.113177_113178delinsTG , LRG_459:g.113177_113178delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.853_854delinsTG
ENST00000683393.1:c.1750_1751delinsTG	ENSP00000508654.1:n.1750_1751delinsTG
ENST00000683760.1:c.1935_1936delinsTG	ENSP00000507765.1:p.Phe645=
ENST00000321117.10:c.2604_2605delinsTG MANE Select	ENSP00000324375.5:p.Phe868=
ENST00000264709.7:c.2604_2605delinsTG	ENSP00000264709.3:p.Phe868=
ENST00000321117.9:c.2604_2605delinsTG	ENSP00000324375.5:p.Phe868=
ENST00000380746.8:c.2037_2038delinsTG	ENSP00000370122.4:p.Phe679=
ENST00000380756.7:c.*457_*458delinsTG	ENSP00000370132.3:n.*457_*458delinsTG
ENST00000402667.1:c.1935_1936delinsTG	ENSP00000384237.1:p.Phe645=
NM_022552.4:c.2604_2605delinsTG , LRG_459t1:c.2604_2605delinsTG	NP_072046.2:p.Phe868=
NM_153759.3:c.2037_2038delinsTG , LRG_459t2:c.2037_2038delinsTG	NP_715640.2:p.Phe679=
NM_175629.2:c.2604_2605delinsTG , LRG_459t4:c.2604_2605delinsTG	NP_783328.1:p.Phe868=
XM_005264175.3:c.2604_2605delinsTG	XP_005264232.1:p.Phe868=
XM_005264177.3:c.1935_1936delinsTG	XP_005264234.1:p.Phe645=
XM_006711958.2:c.2160_2161delinsTG	XP_006712021.1:p.Phe720=
XM_011532662.1:c.2457_2458delinsTG	XP_011530964.1:p.Phe819=
XM_011532663.1:c.2439_2440delinsTG	XP_011530965.1:p.Phe813=
XM_011532665.1:c.2148_2149delinsTG	XP_011530967.1:p.Phe716=
XM_011532666.1:c.2076_2077delinsTG	XP_011530968.1:p.Phe692=
XM_011532667.1:c.1935_1936delinsTG	XP_011530969.1:p.Phe645=
NM_001320893.1:c.2148_2149delinsTG	NP_001307822.1:p.Phe716=
NR_135490.1:n.3141_3142delinsTG
XM_005264175.5:c.2604_2605delinsTG	XP_005264232.1:p.Phe868=
XM_005264177.4:c.1935_1936delinsTG	XP_005264234.1:p.Phe645=
XM_011532662.2:c.2457_2458delinsTG	XP_011530964.1:p.Phe819=
XM_011532663.2:c.2439_2440delinsTG	XP_011530965.1:p.Phe813=
XM_011532666.2:c.2076_2077delinsTG	XP_011530968.1:p.Phe692=
XM_011532667.3:c.1935_1936delinsTG	XP_011530969.1:p.Phe645=
XM_017003526.1:c.2604_2605delinsTG	XP_016859015.1:p.Phe868=
XM_017003527.1:c.1935_1936delinsTG	XP_016859016.1:p.Phe645=
XR_001738657.1:n.2811_2812delinsTG
NM_001375819.1:c.1935_1936delinsTG	NP_001362748.1:p.Phe645=
NR_135490.2:n.3034_3035delinsTG
NM_022552.5:c.2604_2605delinsTG MANE Select	NP_072046.2:p.Phe868=