Canonical Allele Identifier: CA1239262753

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244192A= , CM000664.2:g.25244192A=	GRCh38
NC_000002.11:g.25467061A= , CM000664.1:g.25467061A=	GRCh37
NC_000002.10:g.25320565A=	NCBI36
NG_029465.2:g.103399T= , LRG_459:g.103399T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.133T=
ENST00000683393.1:c.960T=	ENSP00000508654.1:n.960T=
ENST00000683760.1:c.1145T=	ENSP00000507765.1:p.Leu382=
ENST00000321117.10:c.1814T= MANE Select	ENSP00000324375.5:p.Leu605=
ENST00000264709.7:c.1814T=	ENSP00000264709.3:p.Leu605=
ENST00000321117.9:c.1814T=	ENSP00000324375.5:p.Leu605=
ENST00000380746.8:c.1247T=	ENSP00000370122.4:p.Leu416=
ENST00000380756.7:c.1814T=	ENSP00000370132.3:p.Leu605=
ENST00000402667.1:c.1145T=	ENSP00000384237.1:p.Leu382=
ENST00000474887.5:n.133T=
NM_022552.4:c.1814T= , LRG_459t1:c.1814T=	NP_072046.2:p.Leu605=
NM_153759.3:c.1247T= , LRG_459t2:c.1247T=	NP_715640.2:p.Leu416=
NM_175629.2:c.1814T= , LRG_459t4:c.1814T=	NP_783328.1:p.Leu605=
XM_005264175.3:c.1814T=	XP_005264232.1:p.Leu605=
XM_005264177.3:c.1145T=	XP_005264234.1:p.Leu382=
XM_006711957.2:c.1814T=	XP_006712020.1:p.Leu605=
XM_006711958.2:c.1370T=	XP_006712021.1:p.Leu457=
XM_011532662.1:c.1667T=	XP_011530964.1:p.Leu556=
XM_011532663.1:c.1649T=	XP_011530965.1:p.Leu550=
XM_011532664.1:c.1814T=	XP_011530966.1:p.Leu605=
XM_011532665.1:c.1358T=	XP_011530967.1:p.Leu453=
XM_011532666.1:c.1286T=	XP_011530968.1:p.Leu429=
XM_011532667.1:c.1145T=	XP_011530969.1:p.Leu382=
XM_011532668.1:c.1814T=	XP_011530970.1:p.Leu605=
NM_001320893.1:c.1358T=	NP_001307822.1:p.Leu453=
NR_135490.1:n.2152T=
XM_005264175.5:c.1814T=	XP_005264232.1:p.Leu605=
XM_005264177.4:c.1145T=	XP_005264234.1:p.Leu382=
XM_011532662.2:c.1667T=	XP_011530964.1:p.Leu556=
XM_011532663.2:c.1649T=	XP_011530965.1:p.Leu550=
XM_011532664.2:c.1814T=	XP_011530966.1:p.Leu605=
XM_011532666.2:c.1286T=	XP_011530968.1:p.Leu429=
XM_011532667.3:c.1145T=	XP_011530969.1:p.Leu382=
XM_017003526.1:c.1814T=	XP_016859015.1:p.Leu605=
XM_017003527.1:c.1145T=	XP_016859016.1:p.Leu382=
XR_001738657.1:n.2091T=
NM_001375819.1:c.1145T=	NP_001362748.1:p.Leu382=
NR_135490.2:n.2045T=
NM_022552.5:c.1814T= MANE Select	NP_072046.2:p.Leu605=