Canonical Allele Identifier: CA2497029011

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234296_25234297insGGG , CM000664.2:g.25234296_25234297insGGG	GRCh38
NC_000002.11:g.25457165_25457166insGGG , CM000664.1:g.25457165_25457166insGGG	GRCh37
NC_000002.10:g.25310669_25310670insGGG	NCBI36
NG_029465.2:g.113294_113295insCCC , LRG_459:g.113294_113295insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.970_971insCCC
ENST00000683393.1:c.1867_1868insCCC	ENSP00000508654.1:n.1867_1868insCCC
ENST00000683760.1:c.2052_2053insCCC	ENSP00000507765.1:p.Glu684_Tyr685insPro
ENST00000321117.10:c.2721_2722insCCC MANE Select	ENSP00000324375.5:p.Glu907_Tyr908insPro
ENST00000264709.7:c.2721_2722insCCC	ENSP00000264709.3:p.Glu907_Tyr908insPro
ENST00000321117.9:c.2721_2722insCCC	ENSP00000324375.5:p.Glu907_Tyr908insPro
ENST00000380746.8:c.2154_2155insCCC	ENSP00000370122.4:p.Glu718_Tyr719insPro
ENST00000380756.7:c.*574_*575insCCC	ENSP00000370132.3:n.*574_*575insCCC
ENST00000402667.1:c.2052_2053insCCC	ENSP00000384237.1:p.Glu684_Tyr685insPro
NM_022552.4:c.2721_2722insCCC , LRG_459t1:c.2721_2722insCCC	NP_072046.2:p.Glu907_Tyr908insPro
NM_153759.3:c.2154_2155insCCC , LRG_459t2:c.2154_2155insCCC	NP_715640.2:p.Glu718_Tyr719insPro
NM_175629.2:c.2721_2722insCCC , LRG_459t4:c.2721_2722insCCC	NP_783328.1:p.Glu907_Tyr908insPro
XM_005264175.3:c.2721_2722insCCC	XP_005264232.1:p.Glu907_Tyr908insPro
XM_005264177.3:c.2052_2053insCCC	XP_005264234.1:p.Glu684_Tyr685insPro
XM_006711958.2:c.2277_2278insCCC	XP_006712021.1:p.Glu759_Tyr760insPro
XM_011532662.1:c.2574_2575insCCC	XP_011530964.1:p.Glu858_Tyr859insPro
XM_011532663.1:c.2556_2557insCCC	XP_011530965.1:p.Glu852_Tyr853insPro
XM_011532665.1:c.2265_2266insCCC	XP_011530967.1:p.Glu755_Tyr756insPro
XM_011532666.1:c.2193_2194insCCC	XP_011530968.1:p.Glu731_Tyr732insPro
XM_011532667.1:c.2052_2053insCCC	XP_011530969.1:p.Glu684_Tyr685insPro
NM_001320893.1:c.2265_2266insCCC	NP_001307822.1:p.Glu755_Tyr756insPro
NR_135490.1:n.3258_3259insCCC
XM_005264175.5:c.2721_2722insCCC	XP_005264232.1:p.Glu907_Tyr908insPro
XM_005264177.4:c.2052_2053insCCC	XP_005264234.1:p.Glu684_Tyr685insPro
XM_011532662.2:c.2574_2575insCCC	XP_011530964.1:p.Glu858_Tyr859insPro
XM_011532663.2:c.2556_2557insCCC	XP_011530965.1:p.Glu852_Tyr853insPro
XM_011532666.2:c.2193_2194insCCC	XP_011530968.1:p.Glu731_Tyr732insPro
XM_011532667.3:c.2052_2053insCCC	XP_011530969.1:p.Glu684_Tyr685insPro
XM_017003526.1:c.2721_2722insCCC	XP_016859015.1:p.Glu907_Tyr908insPro
XM_017003527.1:c.2052_2053insCCC	XP_016859016.1:p.Glu684_Tyr685insPro
XR_001738657.1:n.2928_2929insCCC
NM_001375819.1:c.2052_2053insCCC	NP_001362748.1:p.Glu684_Tyr685insPro
NR_135490.2:n.3151_3152insCCC
NM_022552.5:c.2721_2722insCCC MANE Select	NP_072046.2:p.Glu907_Tyr908insPro